You are on page 1of 40

European Heart Journal (2001) 22, 1642–1681

doi:10.1053/euhj.2001.2782, available online at on

Task Force Report

Diagnosis and management of aortic dissection*

Recommendations of the Task Force on Aortic Dissection, European
Society of Cardiology†
R. Erbel (Chairman), F. Alfonso, C. Boileau, O. Dirsch, B. Eber, A. Haverich,
H. Rakowski, J. Struyven, K. Radegran, U. Sechtem, J. Taylor, Ch. Zollikofer.
Internal reviewers: W. W. Klein, B. Mulder and L. A. Providencia

Table of contents Magnetic resonance imaging ...............................1661

Aortography ........................................................1662
Page Intravascular ultrasound......................................1663
Preamble ..................................................................1642 Surgical and interventional therapy ........................1664
Introduction.............................................................1643 Surgical therapy ...................................................1664
Aortic wall disease...................................................1643 Interventional therapy by percutaneous stenting
Inherited disease ..................................................1643 and/or percutaneous fenestration.....................1668
Aortic disease in infancy and childhood .............1645 Indications for stent placement and fenestration.1668
Ageing of the aorta..............................................1645 Interventional techniques ....................................1669
Aetiology of aortic aneurysm and dissection ......1647 Results of interventional therapy.........................1670
Aortic dissection staging .........................................1648 Complications of interventional therapy .............1670
class 1 — classical aortic dissection .....................1649 Follow-up in aortic dissection .................................1670
class 2 — intramural haemorrhage/haematoma...1649 Natural history of aortic dissection and
class 3 — subtle/discrete aortic dissection............1650 prognosis ..........................................................1670
class 4 — plaque rupture/ulceration.....................1650 Follow-up in Marfan patients .............................1671
class 5 — traumatic/iatrogenic aortic dissection ..1651 Imaging for follow-up studies..............................1672
Clinical management ...............................................1651 Reoperation .........................................................1672
Clinical features ...................................................1651
Initial diagnostic steps in the emergency room ...1652
Initial therapeutic decisions .................................1653 Preamble
Diagnostic requirements ..........................................1654
Evolving — acute aortic dissection ......................1654 Provisional guidelines were prepared by the ESC Task
Additional information........................................1657 Force on Aortic Dissection, as suggested by the com-
Imaging modalities ..................................................1658 mittee for Scientific Clinical Initiatives and approved by
Transthoracic/transoesophageal echocardiography the ESC Board at its meeting on 17 June 1997.
(TTE/TEE) .......................................................1659 This Task Force consists of 11 members, including
Computed tomography........................................1660 representatives of the European Association of Radiol-
ogy, and the European Society of Pediatric Cardiology,
Manuscript submitted 24 April 2001, and accepted 2 May 2001. as well as one member appointed by the American
College of Cardiology in order to gain ACC endorse-
*This document has been reviewed by members of the Committee ment. The members were all appointed by the Board of
for Scientific and Clinical Initiatives and by members of the Board the ESC upon suggestions made by the committee for
of the European Society of Cardiology (see Appendix 2), who Scientific Clinical Initiatives. In addition, controversial
approved the document in the year 2001. The document received issues were discussed between the members on an e-mail
the ACC Endorsement by the Board of Trustees of the American
College of Cardiology in the year 2001 (see Appendix 3).The full
platform as well as via telephone conferences.
text of this document is available on the website of the European Review of the literature and position papers were
Society of Cardiology in the section ‘Scientific Information’, prepared. At the request of the committee of Scientific
Guidelines and the ACC is listing the document under ‘ACC Clinical Initiatives, the Task Force delineations were
Endorsement’ on their website with a link to the ESC website. presented at the congress of the ESC in August 1999 by
†For affiliations of Task Force Member see Appendix 1. U. Sechtem in the conference on emerging guidelines.

0195-668X/01/221642+40 $35.00/0  2001 The European Society of Cardiology

Task Force Report 1643

Aortic disease

– inherited
– degenerative
– atherosclerotic
– inflammatory
– traumatic
– toxic

Intramural Subtle, Plaque rupture Trauma

haemorrhage/ discrete dissection plaque ulceration Class 5
haematoma Class 3 Class 4
Class 2

Aortic dissection (AD)

Aortic rupture
Class 1
Communicating AD
Non-communicating AD


Figure 1 Schematic illustration of different aortic disease aetiologies which can

result in aortic dissection including progression or regression of the disease.

Finally, the document was distributed for correction Despite this rapid progress, overall agreement about
and endorsement to all members and intermittently the strategy for patient management has not yet been
reviewed for consistency by internal reviewers. An effort achieved. For this reason, this Task Force obtained
was made to include all relevant evidence relating to the opinions from a wide variety of experts with the goal of
diagnosis and treatment of aortic dissection. The mem- formulating recommendations for the best diagnostic
bers were aware of the fact, that for diagnostic tests and strategies to be followed. The diagnostic process was to
surgical as well as interventional procedures related to be based on clinical assessment and the use of the
aortic dissection, no evidence-based medical data for different imaging techniques available in order to estab-
group A and B were available, so that a grading lish a rapid and correct diagnosis while avoiding diag-
concerning consensus between the members was chosen. nostic overkill. Finally, the Task Force will comment
Grading CI meant consensus of all members, grade CII on therapeutic strategies in patients with acute aortic
consensus of the majority of the members, but with data syndromes.
not supporting this decision, grade CIII no consensus, no
or little data available supporting this view.
Aortic wall disease
All mechanisms (Fig. 1) that weaken the aortic wall, the
Introduction aortic lamina media in particular, lead to higher wall
stress, which can induce aortic dilatation and aneurysm
Cardiovascular diseases are the major cause of death in formation, eventually resulting in aortic dissection or
the majority of the developed countries and in many rupture.
developing countries, as reported by the Task Force
of the European Society of Cardiology and proven by Inherited disease
European cardiovascular mortality and morbidity
statistics[1]. Three major inherited disorders are found in this group:
Aortic diseases contribute to the high overall cardio- Marfan’s syndrome, Ehler-Danlos syndrome and other
vascular mortality. New imaging modalities — familial forms of thoracic aortic aneurysm and dissection.
transoesophageal echocardiography, magnetic reso-
nance imaging, helical computed tomography, electron Marfan’s syndrome
beam computed tomography — were introduced during Marfan’s syndrome[7,8] is an autosomal dominant con-
the last decade. These new imaging techniques allow nective tissue disorder with an estimated incidence of
better and earlier diagnosis of aortic diseases even in 1/5000; although more than 25% of cases are probably
emergency situations. These new imaging techniques sporadic. The syndrome involves many systems: skeletal,
have changed patient management during recent years, ocular, cardiovascular, pulmonary, skin and integu-
allowing more rapid diagnosis and decision making[2–6]. ment, and dura. In 1986, an international group of

Eur Heart J, Vol. 22, issue 18, September 2001

1644 Task Force Report

experts agreed upon diagnostic criteria to distinguish terized. There are no well-founded figures on the preva-
Marfan’s syndrome from related disorders. This criteria lence of EDS. An estimated incidence of 1/5000 births is
set is currently referred to as the ‘Berlin nosology’[7]. often stated; this is an aggregate frequency for the
This nosology did not fit in many individual cases and disease. There is no racial or ethnic predisposition[18].
revised criteria were recently proposed, known as the Aortic involvement is seen primarily in EDS type IV[19],
new ‘Gent nosology’[8]. These new criteria include more which is transmitted in an autosomal dominant fashion.
stringent requirements for diagnosing Marfan’s syn- However, approximately 50% of cases are new mu-
drome in relatives of an unequivocally affected individ- tations[19]. In the recently revised nosology, EDS type IV
ual. Particular attention is paid to skeletal involvement is the only member of the ‘EDS vascular type’[20]. The
as a major criterion if at least four of eight typical disease is caused by structural defects in the pro1(III)
manifestations are present, also to the potential con- chain of collagen type III encoded by the COL3A1 gene
tribution of molecular analysis to the diagnosis of located on chromosome 2q31[21,22].
Marfan’s syndrome and the delineation of criteria for
diagnosing other inherited conditions that overlap
with Marfan’s syndrome. Since collagen and elastin Summary
abnormalities are a prominent feature of this disorder, Aortic involvement is typical for Ehler-Danlos syn-
Marfan’s syndrome was long considered a defect of drome, a connective tissue disorder characterized by
either one of these. However, protein and gene studies articular hypermobility, skin hyperextensibility and
demonstrated conclusively that neither one was in- tissue fragility. The disease is caused by structural
volved. Sakai and co-workers identified a new extra- defects in the pro -1 (III) chain of collagen type III.
cellular matrix protein which they named ‘fibrillin’[9].
This protein is the major constituent of microfibrils
found in the extracellular matrix, as either isolated Annuloaortic ectasia and familial aortic dissection
aggregates or closely associated with elastin fibres. To The term annuloaortic ectasia was first used in 1961 by
date more than 100 different mutations have been ident- Ellis et al. to describe a clinical feature, now recognized
ified in the fibrillin-1 gene in patients with Marfan’s as a condition affecting 5% to 10% of patients who
syndrome[10]. The mutations are found in complete and undergo aortic valve replacement for pure aortic regur-
incomplete forms of Marfan’s syndrome but also in a gitation[23]. Two recent studies have analysed familial
spectrum of overlapping diseases, some of which are also aggregation of thoracic aortic dilatation and dissection.
associated with aortic dissection: the Shprintzen- The relative risk of a patient’s father, brothers and
Goldberg syndrome[11], familial or isolated forms of sisters developing aortic aneurysms was 1·8, 10·9 and
aortic aneurysms[12] and the ‘MASS’ phenotype[13]. 1·8, respectively[10]. This report also supports evidence of
These results define the new molecular group of ‘type 1 a sex-linked disease process. In 38·5% of the families
fibrillinopathies’[14]. there was evidence of autosomal dominant transmission,
The clinical variability seen in Marfan’s syndrome is in 23·1% of autosomal dominant or X-linked and in
only partly explained by the great number of mutations 26·9% of either an autosomal or X-linked recessive
identified in the fibrillin-1 gene. Genetic heterogeneity mode[24]. These reports not only underscore the impor-
and the involvement of a second gene (MFS2 for tance of familial aggregation but also the very probable
Marfan syndrome type 2)[15] was demonstrated in a existence of genetic heterogeneity.
French family. Five mutations in the FBN1 gene have now been
The percentage of cases of Marfan’s syndrome associ- identified in patients presenting with either sporadic or
ated with mutations in MFS2 is unknown. However, familial forms of thoracic aortic aneurysms and dissec-
through protein studies, several teams have established tion[13,25]. Other genes may also be involved. Histologi-
that between 7% and 16% of patients with Marfan’s cal examination of the aortic wall reveals loss of elastic
syndrome have normal fibrillin metabolism[16,17]. fibres, deposits of mucopolysaccharide-like material and
cystic medial anomalies, as is also found in patients with
Marfan’s syndrome[26]. No abnormalities of types I and
Summary III collagen or of fibrillin were found in fibroblast
Marfan’s syndrome displays a wide clinical vari- cultures. Furthermore, indirect immunofluorescence
ability. A number of mutations have been identified, studies of the microfibrillar fibre array did not reveal
particularly for the fibrillin-1 (FBN-1) gene. Genetic findings typically associated with Ehlers-Danlos or
criteria are helpful for identifying incomplete forms Marfan’s syndrome.
of the Marfan syndrome.
Annuloaortic ectasia is diagnosed in 5%–10% of
Ehler-Danlos syndrome patients undergoing aortic valve replacement for
Ehler-Danlos syndrome (EDS) is a heterogeneous group aortic regurgitation. Familial aggregation of tho-
of hereditable connective tissue disorders characterized racic aortic dilatation and dissection is present. No
by articular hypermobility, skin hyperextensibility and abnormal type I and III collagen or fibrillin is found.
tissue fragility. Eleven types of EDS have been charac-

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1645

Abdominal aortic aneurysms and dissection

Abdominal aortic aneurysm formation or dissection is
uncommon before the sixth decade. A high proportion
of cases are symptomatic, and the process is very often 4
associated with more proximal aortic involvement[27]. AO 3
Many studies reported familial aggregation of abdomi- 2
nal aortic aneurysms[28]. The risk among people with an
affected first-degree relative was estimated to be 11·6- 1
fold. More patients are women; affected men tend to be LV
younger than affected women. The risk of rupture seems
to be strongly correlated with familial disease and 63%
are female and 37% male[29]. Segregation analyses of
data from 91 families revealed that the disease was very LA
likely determined by a major autosomal diallelic locus
and a recessive disease-causing allele[30]. An autosomal
dominant pattern with a frequency of 1/250 for the
morbid allele and an age-related penetrance no higher
than 0·4 was described in 313 pedigrees[31].
The disease is probably very heterogeneous at the Figure 2 Schematic presentation of the longitudinal par-
genetic level. Furthermore, careful examination of asternal view with four regions where aortic diameters are
measured for follow-up analysis in Marfan’s syndrome.
the pedigrees often reveals involvement not only of the LV=left ventricle; LA=left atrium; 1=valve annulus;
abdominal aorta but also disease in its more proximal 2=aortic sinuses; 3=sinotubular junction; 4=proximal
segments, as well as other clinical features suggestive of ascending artery. (Reprinted from Am J Cardiol, Volume
Marfan’s or Ehlers-Danlos syndrome. Today it is there- 64, Roman MJ, Devereux RB, Kramer, Fox R,
fore difficult to differentiate pure familial forms of O’Loughlin J. Two-dimensional echocardiographic aortic
abdominal aortic aneurysm/dissection from thoracic dimensions in children and adults, pp. 507–512 with
aortic aneurysms/dissection with an abdominal compo- permission from Excerpta Medica Inc.)
nent. This is underscored by the fact that the only
dimensions. This was reported in a large series of cardiac
molecular defect reported to date is that of a mutation
operations in children with Marfan’s syndrome[40]. A
within the COL3A1 gene[32]. In fact, many candidate
close association seems to be present between bicuspid
genes have been investigated that encode various colla-
aortic valves and aortic dilatation resulting in aortic
gens, fibrillins, fibrullins, microfibril-associated glyco-
regurgitation, aneurysm formation and aortic dissection.
proteins, matrix metalloproteinases and their inhibitors,
Dissection has been reported in association with
but no mutation has been identified.
coarctation of the aorta, both above and below the
coarctation site. This complication is not seen in child-
Aortic disease in infancy and childhood hood, but as a complication of untreated coarctation —
usually in the third decade or later and in association
The aortic diameter increases steadily throughout life.
with hypertension. Dissection involving the descending
Standard measurement locations for the aortic root are
aorta below the coarctation site is reported as a compli-
described for children (Fig. 2). Nomograms relating
cation of pregnancy[41]. Dissection also occurs in young
aortic size to body surface area have been published
adults, but not in children with a bicuspid aortic valve
(Fig. 3)[33].
and ascending aortic dilatation[42].
Aortic dissection is rare in infants and children
Although homocystinuria is associated with a pheno-
younger than 16 years, and is not always associated with
type similar to Marfan’s syndrome, the vascular lesions
Marfan’s syndrome or other connective tissue disorders.
tend to be of thrombotic or occlusive nature[43]. There
Only two cases occurring in the Marfan population were
are no reports of abdominal aortic dissection in child-
described during the last 10 years[33,34]. Dissection has,
hood, but abdominal aortic aneurysms are recorded[44].
however, been reported in normal infants following
infection[35], and as a consequence of surgical trauma[36].
Primary balloon dilatation of aortic coarctation as well Summary
as dilatation of re-coarctation may produce damage to Standard measurements and normograms are
the aorta with subsequent development of an aneurysm. helpful for assessing aortic root size related to body
A degree of intimal tearing and dissection can always surface area. Aortic dissection is rare in infants
occur[37]. Dissection originating from the site of aortic and children. Dissection has been reported with
cannulation, particularly if the aortic wall is thin, is a dilatation of aortic coarctation and recoarctation.
recognized complication of cardiopulmonary bypass[38].
Even in Marfan’s syndrome aortic dissection is not Ageing of the aorta
always associated with aneurysmal dilatation of the
aortic root[39], and dissection may originate from an area Normal aortic values have been reported for adults
of non-dilated aorta, irrespective of the aortic root (Table 1). The expansion rate over 10 years is about

Eur Heart J, Vol. 22, issue 18, September 2001

1646 Task Force Report

Region 1 Region 2

Dimension (cm) ± SD

Dimension (cm) ± SD
2·0 3·0




0·0 0·5 1·0 2·5 2·0 0·0 0·5 1·0 2·5 2·0
2 2
BSA (m ) BSA (m )
5·0 5·0
Region 3 Region 4

4·0 4·0
Dimension (cm) ± SD

Dimension (cm) ± SD

3·0 3·0

2·0 2·0

1·0 1·0

0·0 0·5 1·0 2·5 2·0 0·0 0·5 1·0 2·5 2·0
2 2
BSA (m ) BSA (m )
Figure 3 Aortic diameter changes related to body surface area (BSA) for the four different regions illustrated
in Fig. 2. Useful for follow-up studies and detection of abnormal enlargement of the aorta in Marfan’s
syndrome. (Reprinted from Am J Cardiol, Volume 64, Roman MJ, Devereux RB, Kramer, Fox R,
O’Loughlin J. Two-dimensional echocardiographic aortic dimensions in children and adults, pp. 507–512 with
permission from Excerpta Medica Inc.)

1-2 mm[49,50]. Factors that weaken the aortic wall can aneurysm 3·13·2 mm . year 1[54]. Interestingly, aortic
lead to aneurysm formation. According to the law of La diameters in cases with and without dissection were
Place (=pr/2h), wall stress () in a thin wall model is found to be the identical (6 cm vs 6·4 cm)[55]. The same
directly proportional to pressure (p) and radius (r) and holds true for Marfan’s syndrome: this means that
inversely proportional to vessel wall thickness (h). This ascending aortic diameters are 7·4 cm (5·6–10·0 cm) in
makes hypertension as well as cystic media necrosis dissection cases and 6·9 cm (5·3–9·0 cm) in cases without
factors related to the development of aortic disease[51–53]. dissection[39,56,57]. A ratio of the diameter of the aneu-
The expansion rate of aneurysm in the ascending aorta rysm to the normal aorta of less than 2·2 indicates a
is about 1·31·2 mm . year 1 and in the abdominal lower risk for rupture of the abdominal aorta[58]. The

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1647

Table 1 Normal aortic dimensions in adults Intimal thickening increases the distance between the
endothelial layer and the media, compromising the
Diameter nutrient and oxygen supply. Adventitial fibrosis may
Aortic annulus obstruct vessels feeding small intramural vasa vasorum.
Male 2·60·3 cm TTE[33]
Female 2·30·2 cm TTE[33]
Reduced nutritional supply of the media results in
Sinus of Valsalva medial thinning secondary to necrosis — primarily due
Male 3·40·3 cm TTE[33] to necrosis of the smooth muscle cells. Another conse-
Female 3·00·3 cm TTE[33] quence is a fibrotic change in the elastic structures of the
Aortic root <3·7 cm TTE[33] medial layer[64]. All these changes contribute to in-
Proximal ascending aorta
Male 2·90·3 cm TTE[33]
creased vessel stiffness and to higher vulnerability to
Female 2·60·3 cm TTE[33] shear stress, eventually leading to the formation of
Ascending aorta 1·4–2·1 cm . m 2 TEE[45] aneurysms and dissections, especially in the infrarenal
<3·8 cm (2·5–3·8) CT[2] aorta[66].
<3·7 cm TTE[46] In cases of aortic aneurysms severe aortic athero-
Descending aorta 1·0–1·6 cm . m 2 TEE[45]
sclerosis involves more than 70% of the surface in over
<2·8 cm (1·7–2·8) CT[2]
Wall thickness 90% of the patients[68]. Ruptures are more common in
Aortic wall <4 mm CT[47] the ascending aorta (65%) and less frequent in the
<3 mm Angio[48] abdominal aorta (32%). Fusiform thoracic aortic aneu-
<4 mm TEE[49] rysms have a higher rupture risk (61%) compared to
abdominal aortic aneurysms[67]. Aortic rupture is found
in 0·9% of cases of sudden death. Aortic dissections are
present in 62% of these patients, atherosclerotic aneu-
ratio was 2·7 in symptomatic patients and 3·4 in a group rysms in 37% and false aneurysms in 1·6%[67].
with evidence of rupture[59]. Thus, the risk of aortic The main risk factor for aneurysm formation in
aneurysmal rupture seems to be related to the aortic atherosclerosis is hypertension, which is found in 85% of
diameter (Table 2). An increase in the aortic diameter of those with ruptured or 52% of those with non-ruptured
pre-existing aneurysms is lower in the thoracic than in aneurysms[67]. The risk factors, e.g. smoking and hyper-
the abdominal aorta[52], a fact possibly related to the cholesterolaemia, are also associated with an increased
vasa vasorum being absent in the abdominal aorta[64]. If incidence of aortic aneurysms[68]. However, 60% of
aortic dissection is present, an expansion rate of patients have a cholesterol level of less than
5–20 mm within 3 years can be expected. The rate 240 mg . dl 1 (6·2 mmol . l 1)[68].
is 1 mm . year 1 for non-communicating and Secondary to high-speed accidents, 15%–20% of
2–3 mm . year 1 for communicating dissection[65]. deaths are related to aortic trauma. About 95% of the
injuries occur at the site of greatest stress, the aortic
isthmus, only 5% at the ascending aorta[69]. Aortic
Aetiology of aortic aneurysm and dissection disruption can be limited to the intima or include the
Atherosclerosis is the main cause of aortic aneu- entire wall. Chronic aneurysms tend to become sympto-
rysms[66,67]. Atherosclerosis leads to gross thickening of matic or rupture within 5 years. Aortic rupture will
the intima. The intima shows massive fibrosis and calci- ultimately occur in most patients mainly after forming
fication, and increased amounts of extracellular fatty pseudoaneurysms, which can enlarge and compress sur-
acids. The integrity of this layer can be compromised by rounding structures like the pulmonary artery[70]. Aortic
the extracellular matrix being degraded by histiocytic rupture after blunt chest trauma is frequently associated
cells. Additional degenerative changes can develop with myocardial contusion which can lead to cardiac
within the fibrous tissue. These changes are character- failure, myocardial infarction, and tamponade.
ized by reduced cellularity and collagen fibre hyaliniz- Aneurysm formation and aortic rupture can also
ation. Both mechanisms may lead to intimal rupture, occur after aortic surgery and even after cardio-
most often at the edges of plaques. pulmonary resuscitation[71–73]. Extracorporal shock

Table 2 Aortic diameters in aneurysms with or without dissection: indications for surgery in different patient groups

Authors Results Patient population and method

Lemon[60] No difference in diameter With and without dissection (angiography)

McDonald et al.[61] >5·5 cm Marfan’s syndrome — surgery
Roberts[51] >5·3 cm Marfan’s syndrome — dissection
White et al.[62] >6·0 cm Computed tomography (CT)
Tijon-A-Meeuw[63] 0·2–0·4 cm/year Aortic diameter increase
>5 cm surgery, as 30% rupture in <2 years
Sütsch[55] Surgery before 6 cm is reached Transoesophageal echocardiography

Eur Heart J, Vol. 22, issue 18, September 2001

1648 Task Force Report

Table 3 Types of vasculitis predominately involving large and medium-sized


(1) Takayasu’s aorto-arteritis

(2) Giant cell arteritis
(a) Temporal arteritis
(b) Disseminated giant cell arteritis
(c) Primary angitis of the central nervous system (considered by many as a viral infection)
(3) Behcet’s disease
(4) Aortitis associated with rheumatoid disease
(5) Inflammatory abdominal aortic aneurysm (aetiology unknown — probably an immune
response to lipids infiltrating the aortic wall)
(6) Aortitis in relation with retroperitoneal fibrosis (Ormond’s disease)

waves can produce aortic injury as well[74]. Another

possible cause of trauma is cardiac catheterization as a Summary
diagnostic or interventional procedure[75]. Aortic dis- Hypertension is a main risk factor of aortic sclerosis
section may be observed in patients who underwent and subsequent aortic aneurysm formation and
prior aortic valve replacement. The interval between aortic dissection.
valve replacement and dissection varies greatly[76,77]. Smoking and hypercholesterolaemia are additional
The mechanism which revealed an area of condensed risk factors.
resistance within the aortic wall may have been the jet 15%–20% of death secondary to high speed
lesion which produced the post stenotic ascending accidents are related to aortic trauma, frequently
aortic dilatation similar to aortic wall disease in aortic associated with myocardial contusion.
stenosis and regurgitation. However, distal aortic Iatrogenic aortic dissection is often related to
dissection has also been observed after aortic valve cardiac catheterization, angioplasty, or surgery.
replacement, suggesting additional risk factors for this Inflammatory diseases can affect the aorta as
occurrence[76,77]. in Takayasu arteritis and syphilis as well as in
Inflammatory diseases can destroy the medial layers Behcet’s or Ormond’s disease.
of the aortic wall and lead to weakening of the aortic Cocaine and amphetamine associated with aortic
wall, hastening expansion and causing higher wall aneurysm formation and dissection are newly
stress. Suppurative bacterial or fungal aortitis is rare. detected aetiologies.
It can cause focal destruction of the vessel wall
with subsequent aneurysm formation and/or rupture.
Autoimmune diseases of the aorta (Table 3) can sev- Aortic dissection staging
erely affect the vasa vasorum, and decrease the blood
supply of the media[78]. Furthermore, inflammatory The Stanford classification of aortic dissection distin-
lesions — as seen in Takayasu arteritis — may develop guishes between type A and type B (Fig. 4)[86,87]. Type A
inside the aortic wall. Such inflammatory lesions con- means the dissection includes the ascending aorta, a type
sist of an inflammatory infiltrate, smooth muscle and B dissection does not involve the ascending aorta. The
fibroblast necrosis, and fibrosis of the vessel wall (for a De Bakey classification subdivides the dissection process
review see:[79]). Inflammation related to infectious dis- further: a type I dissection involves the entire aorta, a
eases, such as luetic aortitis, can lead to similar type II dissection involves the ascending aorta, and
changes. Aortitis is the principal cardiovascular mani- a type III dissection the descending aorta[87]. The first
festation of syphilis, found mainly in the ascending attempt to further subdivide the De Bakey classification
aorta, but distal segments can be involved[80]. was made by Reul and Cooley (Fig. 4), differentiating
Rheumatoid arthritis can also lead to aortitis. Second- from thoracic abdominal type III dissection[88]. Sub-
ary typical aortic dissections are unusual. The diseased dividing into proximal and distal or ascending and
aorta may rupture. Toxic aortic disease is seen in animals descending aortic dissections is also common.
after the administration of beta-aminopropionitrile New studies demonstrated that intramural haemor-
fumarate which leads to changes in the media morpho- rhage, intramural haematoma and aortic ulcers may be
logically similar to mucoid degeneration of the aortic signs of evolving dissections or dissection subtypes.
wall[81]. Other chemicals have been shown to cause cellu- Consequently, a new differentiation (Fig. 5) has been
lar necrosis in the media (for a review see:[82]). The proposed[89].
administration of high doses of zinc can also lead
to aortic dissections in animal models[83]. In humans, class 1: classical aortic dissection with an intimal flap
different drugs such as cocaine and amphetamine between true and false lumen
are associated with aneurysm formation and aortic class 2: medial disruption with formation of intra-
dissection[84,85]. mural haematoma/haemorrhage

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1649

De Bakey I II III
Stanford A A B

Figure 4 Schematic drawing of aortic dissection class 1, subdivided into DeBakey types I, II and III.
Also depicted are Stanford classes A and B with subtypes a and b (subtype depends on the thoracic or
abdominal involvement according to Reul and Cooley[88]).

class 3: discrete/subtle dissection without haematoma, Intramural haematoma/haemorrhage (class 2)

eccentric bulge at tear site
class 4: plaque rupture leading to aortic ulceration, pen- An intramural haematoma is probably the initial lesion
etrating aortic atherosclerotic ulcer with sur- in the majority of cases of cystic medial degeneration.
rounding haematoma, usually subadventitial This leads to aortic dissection in which the intimal tear
class 5: iatrogenic and traumatic dissection seems to be secondary to preceding intramural
All classes of dissection can be seen in their acute and dissection[95–104]. Intramural haematoma/haemorrhage
chronic stages; chronic dissections are considered to be may be the result of ruptured normal-appearing vasa
present if >14 days have elapsed since the acute event or vasorum which are not supported by the surrounding
if they are found occasionally. aortic media or the result of rupture of diseased vasa
vasorum[64,96]. As a dissection the haematoma can ex-
tend along the aorta. The weakened inner wall is sub-
Classic aortic dissection (class 1) jected to the elongating force of the diastolic recoil,
which can result in intimal tears only visible at surgery
Acute aortic dissection is characterized by the rapid or autopsy. Differences in elasticity between the aortic
development of an intimal flap separating the true and fibrous adventitia and the inner more elastic media may
false lumen[51]. Due to the pressure difference the true play an additional role[97]. From class 2 aortic dissection,
lumen is usually smaller than the false lumen. Intimal the class 1 non-communicating classical dissection,
flap tears characterize communicating dissections[6]. which shows all signs of dissection, — an intimal flap, a
However, tears are not always found and non- true and false lumen but no flow within the false lumen
communicating dissections are not uncommon[6,91–99]. In due to the absence of an intimal tear, — has to be
an autopsy study, dissecting aneurysms without tears separated. The class 2 dissection may have an intramural
were found in up to 12% of 311 autopsies[95]. Others haematoma, but also can present as diffuse —
have reported an incidence of 4% in 505 cases[97]. In a haemorrhagic — intramural bleeding, giving the impres-
series of sudden deaths, 67% of patients with dissections sion of wall thickening. If intramural haematoma is
did not have tears[99]. The dissection can spread from present, only a discrete and very localized separation of
diseased segments of the aortic wall in an antegrade or wall layers occurs, which may be very superficial or
retrograde fashion, involving side branches and causing deeply located within the aortic wall: multiple layerings
other complications[6,93,94]. may be observed.

Eur Heart J, Vol. 22, issue 18, September 2001

1650 Task Force Report

Class 1 Class 2

Class 3 Class 4 Class 5

Figure 5 Differentiation of classes 1–5 of aortic dissection. Class 1: classic aortic
dissection with true and false lumen without communication of the two lumina; class 2:
intramural haemorrhage or haematoma; class 3: ulceration of aortic plaque following
plaque rupture; class 4: subtle or discrete aortic dissection with bulging of the aortic
wall; class 5: iatrogenic or traumatic aortic dissection, illustrated by a catheter induced
separation of the intima. (From Svensson LG, Labib SB, Eisenhauser AC, Butterfly
JR. Intimal tear without haematoma. Circulation 99: 1331–6, 1999; American Heart
Association; reproduced with permission.)

The prevalence of intramural haemorrhage and hae- dissection as a consequence of intramural haemor-
matoma in patients with suspected aortic dissection, as rhage and haematoma develops in 28–47% of the
observed by various new imaging techniques, seems to patients[90–92,101,104]. It is associated with aortic rupture
be in the range of 10–30%[90,92,101,104]. in 21–47%; and regression is seen in about 10% of
There are two distinct types of intramural haematoma patients[90–92,101,104].
and haemorrhage:
Type I shows a smooth inner aortic lumen, the
diameter is usually less than 3·5 cm, and the wall thick- Subtle-discrete aortic dissection (class 3)
ness greater than 0·5 cm. Echo-free spaces (seen echo-
The structural weakness can lead either to clinically
cardiographically) as a sign of intramural haematoma
inapparent disease or minor forms of aortic dissection.
are found in only one third of the patients. The mean
Subtle dissection has been described[89] as a partial
longitudinal extent of the haematoma is 11 cm and the
stellate or linear tear of the vessel wall, covered by
echo free spaces show no signs of flow[91].
thrombus. When the partial tear forms a scar, this
Type II occurs in aortic atherosclerosis. A rough inner
constellation is called an abortive, discrete dissection.
aortic surface with severe aortic sclerosis is characteristic;
Partial ruptures of the inner layer of the aorta allow
the aorta is dilated to more than 3·5 cm and calcium
blood to enter the already damaged media and thus
deposits are frequently found. Mean wall thickness is
cause dissection of the aortic wall, eventually leading to
1·3 cm with a range of 0·6–4 cm, and echo free spaces are
a second lumen within the wall, to a rupture or healing
found in 70% of the patients studied. The longitudinal
during follow-up[89].
extension has a range similar to type I haematoma, usually
about 11 cm[91]. Intramural haemorrhages are found more
often in the descending than in the ascending aorta[91]. Plaque rupture/ulceration (class 4)
The fact that intramural haemorrhage and hae-
matoma can lead to aortic dissection has been demon- Ulceration of atherosclerotic aortic plaques can lead to
strated in follow-up studies[90–92,101,104]. Acute aortic aortic dissection or aortic perforation[105–110]. This was

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1651

first observed by computed tomography[105,106]. The Table 4 Aortic dissection — common presenting
new imaging techniques — intravascular ultrasound, symptoms
spiral computed tomography and magnetic resonance
imaging — provide new insights. The ability to diagnose Pain
aortic ulceration has thereby been improved and further Pain alone
Pain with syncope
insight into the pathophysiology of this condition has Pain with signs of congestive heart failure
been gained[107]. The ulcers seem to affect the descending Pain with cerebrovascular accident (stroke)
thoracic aorta, as well as the abdominal aorta, and are Congestive heart failure without pain
not usually associated with extensive longitudinal propa- Cerebrovascular accident without pain
gation or branch vessel compromise[103]. Valvular, peri- Abnormal chest roentgenogram without pain
Pulse loss without pain
cardial or other vascular complications appear rare. The
ulcer may penetrate beyond the intimal border, often
with a nipple-like projection with subjacent type II
intramural haematoma formation[91,108]. The continuous Table 5 Aortic dissection — differential diagnosis
erosion of the atherosclerotic plaque may eventually
violate the internal elastic membrane[106]. False aneu- Acute coronary syndrome with and without ST-elevation
rysms, aortic rupture or dissections may occur[109,110]. Aortic regurgitation without dissection
Aortic aneurysms without dissection
Musculoskeletal pain
Traumatic/iatrogenic aortic dissection Pericarditis
Mediastinal tumours
(class 5) Pleuritis
Pulmonary embolism
Blunt chest trauma usually causes dissection of the Cholecystitis
ascending aorta and/or the region of the ligamentum Atherosclerotic or cholesterol embolism
Botalli at the aortic isthmus. Iatrogenic dissection of the
aorta rarely occurs during heart catheterization. It is
regularly seen following angioplasty of an aortic co-
arctation (in adults), but can also be observed after Clinical management
cross-clamping of the aorta and after intra-aortic bal-
loon pumping[71,75,111,112]. Most catheter-induced dis- Clinical features
sections are retrograde dissections. They will usually
decrease in size as the false lumen thromboses[112].
The main challenge in managing acute aortic dissection
Proximal progression of the coronary dissection into the
is to suspect and thus diagnose the disease as early as
aortic root may be observed[112].
The typical patient with aortic dissection presenting to
an emergency department today is a male in his 60s with
Summary a history of hypertension who suffers with abrupt onset
Stanford classification of chest pain[113–115]. The following clinical manifes-
Type A — dissection of the ascending and descend- tations (Table 4) of acute aortic dissection are present
ing aorta in up to 90% of patients presenting in the emergency
Type B — dissection of the descending aorta room:
De Bakey classification v Pain of abrupt onset with its maximum at the time of
Type 1 — dissection of the entire aorta onset (Table 4). With further extension of the dissec-
Type 2 — dissection of the ascending aorta tion process, the pain may change its location accord-
Type 3 — dissection of the descending aorta ingly. The pain is described as sharp more often than
New classification tearing, ripping, or stabbing[113–115]. In contrast, the
class 1: classical aortic dissection with an intimal pain associated with acute myocardial infarction starts
flap between true and false lumen slowly and gains in intensity with time. It is usually
class 2: medial disruption with formation of intra- more oppressive and dull.
mural haematoma/haemorrhage v In proximal dissections, the pain is usually located
class 3: discrete/subtle dissection without hae- retrosternally, whereas distal dissections are character-
matoma, eccentric bulge at tear site ized by interscapular as well as back pain.
class 4: plaque rupture leading to aortic ulcer- v Hypertension is typically associated with distal aortic
ation, penetrating aortic atherosclerotic dissection.
ulcer with surrounding haematoma, Differential diagnoses need to be taken into account
usually subadventitial (Table 5). One also needs to be aware of less common
class 5: iatrogenic and traumatic dissection presentations. Chest pain may be absent, but this is
Class 1–5 represent a subdivision to the Stanford or usually indicative of chronic aortic dissection. Up to
De Bakey classification 20% of patients with acute aortic dissection may
present with syncope without a history of typical pain or

Eur Heart J, Vol. 22, issue 18, September 2001

1652 Task Force Report

neurological findings[113–115]. Following a period of pain, proximal aortic dissection[113,115,122]. Occasionally, the
cardiac failure may become the main symptom and is murmur can be very faint and the typical wide pulse
usually related to severe aortic regurgitation. Cardiac pressure as well as other peripheral signs of severe aortic
tamponade may result in hypotension and syncope. regurgitation may be absent. Signs of pericardial in-
Syncope may also result from severe pain, obstruction of volvement such as the presence of a pericardial friction
cerebral vessels or activation of aortic baroreceptors. rub, jugular venous distension or a paradoxical pulse
Cerebrovascular manifestations and limb ischaemia with should alert the physician to call for rapid surgical
pulse deficits are caused by obliteration of the peripheral intervention.
vessel by involvement of the vessel origin into the Pleural effusions may be caused by rupture of the
dissection or obliteration of the true lumen by an aorta into the pleural space, the left side is usually
expanding false lumen. Paraplegia may suddenly de- involved. Pleurocentesis reveals the presence of blood
velop as intercostal arteries are separated from the aortic indicating the need for emergency surgery. However, an
lumen by the dissection. Involvement of the renal ar- effusion may simply be the expression of an exudative
teries may result in oliguria or anuria. Further propaga- inflammatory reaction from the dissected aorta and no
tion of the dissection at a later point in time will usually further action is required.
result in another (2nd) attack of the same acute pain as Up to 30% of patients later found to have aortic
at the initial event, and is often associated with a dissection are initially suspected to have other con-
deteriorating clinical picture[115]. When the dissection ditions, such as acute coronary syndromes, non-
results from some form of trauma, albeit iatrogenic, it is dissecting aneurysms, pulmonary embolism, or aortic
the circumstance rather than symptoms that should alert stenosis[112,114,122]. Consequently, the differential diag-
one to that possibility. High fever is not common but nosis of acute aortic dissection should always be consid-
can occur due to the release of pyrogenic substances ered in patients presenting with unexplained syncope,
from the aortic wall. It can persist for a longer period of stroke, acute onset of congestive heart failure, and acute
time and may be misinterpreted as a sign of another ischaemia of extremities or viscera, even when the typi-
inflammatory disease[73,116]. cal chest pain of aortic dissection is not the leading
Persistent abdominal pain, elevation of acute phase symptom (Table 6). In these patients, an imaging pro-
proteins, and increase of lactate dehydrogenese are cedure needs to be carried out as soon as possible to rule
indicators of involvement of the coeliac artery. This is out or to confirm the presence of dissection.
observed in about 8% and involvement of the mesenteric
artery in 8–13%[116,117].
Initial diagnostic steps in the emergency
Physical examination room
Physical examination can provide important clues as to
the presence and origin of the aortic dissection. Whereas Although speed is of utmost importance, an ECG (Table
pulse deficits were found in 50% of patients with proxi- 6) must be acquired in all patients. This test helps
mal aortic dissection in their 70s[114], a large current distinguish acute myocardial infarction, for which
registry of patients with acute aortic dissection reported thrombolytic therapy may be life saving, from aortic
this finding in less than 20% of patients[115]. These pulse dissection, in which thrombolytic therapy may be detri-
phenomena may be transient due to the intimal flap’s mental[123]. Both conditions may coexist as the dissecting
changing position. Neurological deficits (loss of con- membrane may extend into a coronary ostium (usually
sciousness, ischaemic paresis) occur in up to 40% of that of the right coronary artery) causing acute myocar-
patients with proximal aortic dissection[114,117]. On rare dial ischaemia. Such coronary involvement will induce
occasions, symptoms such as vocal chord paralysis in the ECG signs of acute myocardial infarction and this
(caused by compression of the left recurrent laryngeal in turn could result in potentially detrimental admin-
nerve), haemoptysis or haematemesis (due to haemor- istration of thrombolytic therapy. However, a normal
rhage into the tracheobronchial tree or perforation into ECG is present in one third of patients with coronary
the oesophagus)[118], superior vena cava syndrome[119], involvement and most of these patients have non-specific
upper airway obstruction due to compression, Horner’s ST-T segment changes[123]. About 20% of patients with
syndrome (due to compression of the superior cervical type A dissection have ECG evidence of acute ischaemia
sympathetic ganglion), signs suggestive of pulmonary or acute myocardial infarction[123]. These patients with
embolism (if there is extravasation of blood from the suspected aortic disease and ECG evidence of ischaemia
false channel into the common adventitia of the ascend- must undergo diagnostic imaging before thrombolytic
ing aorta and pulmonary artery leads to severe compres- therapy is administered. The chest X-ray is not sufficient
sion of the pulmonary artery[120] ) or signs of mesenteric to rule out aortic dissection[124]. However, diagnostic
or renal ischaemia may be encountered[115,121,122]. If the imaging cannot be performed in all patients presenting
iliac bifurcation is completely obstructed, Leriche’s with myocardial ischaemia, and erroneous admin-
syndrome with pulse loss in both legs will occur, which is istration of thrombolytic therapy may be unavoidable in
typically painless. the occasional patient who is subsequently found to
A diastolic murmur indicative of aortic regurgi- have aortic dissection, but an enlarged mediastinum may
tation is present in about half of the patients with indicate an unsuspected aortic dissection.

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1653

Table 6 Initial management of patients with suspected aortic dissection

Recommendation Class I II III Level of evidence

1. Detailed medical history and complete physical examination (whenever possible) + C

2. Intravenous line, blood sample (CK, TnT(I), myoglobin, WBC, D-dimer, haematocrit, LDH) + C
3. ECG: documentation of ischaemia + C
4. HR and blood pressure monitoring + C
5. Pain relief (morphine sulphate) + C
6. Reduction of systolic blood pressure using beta-blockers (i.v. propranolol, metoprolol, esmolol + C
or labetalol)
7. Transfer to intensive care unit + C
8. In patients with severe hypertension additional vasodilator (i.v. sodium nitroprusside to titrate + C
BP to 100–120 mmHg)
9. In patients with obstructive pulmonary disease, blood pressure lowering with calcium channel + C
10. Imaging in patients with ECG signs of ischaemia before thrombolysis if aortic pathology is + C
11. Chest X-ray + C

The role of the chest X-ray is currently unclear (Table appropriate drug to provide pain relief is morphine
6)[124]. A routine chest X-ray will be abnormal in be- sulphate. Beta-blockers as a group of drugs have the
tween 60%[115] to 90% of cases[113] with suspected aortic most desirable effect of reducing the force of left ven-
dissection and will thus make the diagnosis of aortic tricular ejection (dP/dt) which continues to weaken the
dissection more likely. However, in unstable patients, a arterial wall. Intravenous beta-blockers such as pro-
chest X-ray will result in further delay before instituting pranolol (0·05–0·15 mg per kg of body weight every 4 to
treatment and should thus be omitted. 6 h[127]) or esmolol (administrated at a loading dose of
The often large wound surface and haematoma may 0·5 mg . kg 1 over 2–5 min followed by an infusion of
be reflected in laboratory findings such as elevated 0·10–0·20 mg . kg 1 min 1) can be given. It needs to be
C-reactive protein, mild-to-moderate leukocytosis and remembered that the maximum concentration of es-
slight elevations of bilirubin and lactic acid dehydrogen- molol is only 10 mg . ml 1. The infusion of this agent at
ase[125]. More recently, the biochemical diagnosis of a maximal dose of 0·3 mg . kg 1 min 1 constitutes a
aortic dissection has become possible by identifying substantial volume load. Metoprolol and atenolol are
raised concentrations of smooth muscle myosin heavy also available for intravenous application, but have a
chain[125]. longer half-time. Labetolol, a drug which blocks both
alpha- and beta-adrenergic receptors, can also be used in
Initial therapeutic decisions patients with aortic dissection. In patients with potential
intolerance to beta-blockers (those with bronchial
Every patient with suspected aortic dissection should asthma, bradycardia, signs of heart failure) esmolol (with
undergo diagnostic imaging by one of the techniques its short half life) seems be a reasonable choice to test the
discussed below to rule out the disease. The benefits of patient’s reaction to beta-blockers. There are no data
this strategy outweigh the risks of being harmful to supporting the use of calcium antagonists in these
patients ultimately found to have another condition[126]. patients, but drugs such as verapamil, diltiazem, or
Whilst arranging for appropriate testing, the patient nifedipine may be necessary in order to reduce blood
needs to be moved to an intensive care unit for appro- pressure, particularly in patients with bronchial asthma.
priate monitoring (Table 6). As fluid replacement may If beta-blockade alone does not control hypertension,
become of utmost importance in cases of haemodynamic vasodilators are ideal additional agents to control blood
deterioration, drugs should be infused through a separ- pressure. However, as vasodilators can increase the force
ate intravenous line. In the unstable patient, invasive of left ventricular ejection, they should always be com-
blood pressure monitoring should be provided by bined with beta-blockers (Table 6). While beta-blocking
placing an arterial line to the right radial artery. If agents are usually adequate in patients with slightly
involvement of the brachiocephalic trunk is suspected elevated blood pressure, combination with intravenous
(rarely seen), this line should be placed on the left side. It sodium nitroprusside may be required for more severe
is important to rule out the presence of pseudo- hypertension. The initial dose is 0·25 g . kg 1 min 1.
hypotension due to obstruction of an aortic arch branch. Systolic blood pressure should be titrated to values
Therefore pressure measurement on both arms is between 100 and 120 mmHg. Lowering of systolic blood
important. pressure must be modified if oliguria or neurological
While waiting for diagnostic imaging, it is necessary symptoms develop.
to control pain and reduce systolic blood pressure to In patients with normal or even reduced systolic blood
values between 100 and 120 mmHg (Table 6). The most pressure at presentation, possible volume depletion —

Eur Heart J, Vol. 22, issue 18, September 2001

1654 Task Force Report

Table 7 Management of haemodynamically unstable patients with suspected aortic dissection

Recommendation Class I II III Level of evidence

1. Profound haemodynamic instability: intubation and ventilation + C

2. Transoesophageal echocardiography as the sole diagnostic procedure — call surgeon + C
3. Surgery-based on findings of cardiac tamponade by transthoracic echocardiography + C
4. Pericardiocentesis (lowers intrapericardial pressure (recurrent bleeding!)) + C

which may be the result of blood sequestration in the Table 8 Imaging: diagnostic goals
false lumen or the pleural and pericardial space — has to
be ruled out. Patients with profound haemodynamic + Confirm diagnosis
+ Classify the dissection/delineate the extent
instability (Table 7) need to be intubated and ventilated + Differentiate true and false lumen
without delay. Transoesophageal echocardiography can + Localize intimal tears
be performed as the sole diagnostic procedure in the + Distinguish between communicating and non-communicating
intensive care unit or later in the operating theatre[3,128]. dissection
If speed is vital, transthoracic echocardiography should + Assess side branch involvement (including coronary arteries)
+ Detect and grade aortic regurgitation
be carried out immediately, but the resulting image
+ Detect extravasation (periaortic or mediastinal haematoma,
quality is rarely adequate for decision making. The pleural or pericardial effusion)
echocardiographic finding of cardiac tamponade may
lead to sternotomy and exploratory surgery without
further imaging. Pericardiocentesis (Table 7) as an initial The following methods can confirm the diagnosis with
therapeutic step before surgery may be harmful as this high accuracy. In the large international registry of
reduces intrapericardial pressure and may therefore aortic dissection (IRAD), the first diagnostic step
cause recurrent bleeding[129]. was transthoracic echocardiography (TTE) and trans-
oesophageal echocardiography (TEE) in 33%, computed
tomography (CT) in 61%, magnetic resonance imaging
(MRI) in 2% and angiography in 4%[130]. In 56% TTE/
Aortic dissection has a wide range of clinical presen- TEE, in 18% CT, in 9% MRI and in 17% angiography
tations. Clinical suspicion is required for quick risk were used as secondary techniques. Therefore an average
stratification and management. of 1·8 methods were utilized to diagnose aortic dissec-
Monitoring of heart rate and blood pressure is tion. CT was used in 40%, MR in 30% and angiography
indicated. Beta-blocking therapy and blood press- in 21% of those cases where three methods were
ure lowering medications are started, as well as chosen[130].
sedation and analgesic therapy. The decision for a specific technique depends on two
Monitoring in the intensive care unit should be major factors:
initiated. Fluid replacement may be important. + Availability in emergency situations
Use a separate line for blood pressure lowering. + Experience of the emergency room and imaging staff
Start with beta-blocking agents and add sodium Patients with acute aortic dissections are usually ad-
nitroprussid, if necessary. mitted to the emergency wards of regional hospitals,
In case of haemodynamic instability, the patient where not all methods described in the previous section
should be intubated and transferred to the operat- are available. If aortic dissection is suspected, patients
ing theatre. TEE may be performed prior to transfer should be transferred to a centre with interventional and
or in the operating theatre. surgical back up. Each institution should establish their
guidelines for the most rapid and accurate diagnostic
steps to confirm the diagnosis. The use of two or even
three imaging techniques to diagnose aortic dissection is
Diagnostic requirements (Table 8) excessive and often can lead to unnecessary time loss. As
far as decision making is concerned, only experienced,
Evolving — acute aortic dissection well trained physicians are able to reduce the number of
false diagnoses, which are more likely when the dissec-
Essential information: confirming the diagnosis tion is not the classical class 1 dissection, but a dissection
The demonstration of an intimal flap separating two of class 2–4[131–135]. Data relating the sensitivity and
lumina is the basis for diagnosing aortic dissection class. specificity of the different techniques for various scen-
If the false lumen is completely thrombosed, central arios are quite limited[136–138]. In class 3 dissection, only
displacement of the intimal flap, calcification or separ- aortography — and not TEE, CT, or MRI — may make
ation of intimal layers (Table 9) can be regarded as the physician aware of the presence of a discrete and
definitive signs of aortic dissection[3]. subtle aortic dissection[89].

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1655

Table 9 Differentiate between atherosclerotic aortic aneurysm and aortic dissection

Atherosclerotic aortic
Aortic dissection

Aortic diameter >> >

Wall thickness > (>) normal, except for:
intramural haematoma;
intramural haemorrhage
Luminal surface rough smooth
Thrombus formation lumen false lumen
Floating thrombi ++ false lumen
Displacement of intimal calcifications (+) ++
Signs of slow flow often inside the lumen false lumen

Table 10 Differentiation between communicating and non-communicating aortic dissection

Communicating dissection (c) Non-communicating dissection (nc)

+ Intimal tear + Intima intact

+ Flow within false lumen + No flow in false lumen
+ Phasic motion of the intimal flap + No/or reduced motion of the intimal flap
+ High flow signals in the false lumen + Signs of reduced flow, spontaneous echocardiographic contrast
+ No or incomplete thrombus formation in the false lumen + Thrombus formation in the false lumen — incomplete or complete

Table 11 Aortic dissection: differentiation between true and false lumen

True lumen False lumen

Size true<false most often false>true

Pulsation systolic expansion systolic compression
Flow direction systolic antegrade flow systolic antegrade flow reduced or absent or retrograde flow
Localization within the aortic arch inner contour outer contour
Signs of slow flow rare frequent; depending on degree of communication
Thrombus rare frequent; depending on degree of communication

Tear localization and disease extent the abdomen which used to limit examinations in the
Any therapeutic intervention aims to occlude the entry past. The full extent of the dissection can be visual-
tear (e.g. by stent implantation or grafting), which ized non-invasively by CT, MRI or invasively by
makes tear detection and localization very important. It angiography.
is common to see not just one entry and one reentry, but
multiple tears[94]. The pressure difference between the Classification of aortic dissection
true and false lumen forces the blood from the true to The extent (beginning and end point) of a dissection can
the false lumen and back, but multidirectional flow jets be described by taking wall thickness and the intimal
can be observed[94]. Intimal tears can be visualized flap into account. Depending on flow in the false lumen
directly by TTE, TEE, CT and MRI, but also by or tears in the intimal flap, communicating and non-
angiography[136]. Pulsed Doppler and continuous wave communicating aortic dissections (Tables 10, 11) can be
Doppler can give an estimate of the pressure difference distinguished. Communication is present when forward,
between the false and true lumen. reversed or delayed flow is detected in the false lumen. In
The full extent of aortic dissection can be analysed acute communicating dissections, the intimal flap may
by ultrasonic techniques alone, if echocardiography display strong excursions during the cardiac cycle. Such
is combined with duplex sonography, abdominal movement as well as flow are reduced or absent when
sonography — or even better — intravascular ultra- no communication is present. Depending on the degree
sound. Due to its low image quality, duplex abdominal of communication, thrombus formation may be ob-
sonography cannot be used for unequivocal decision served[6,94]. Spontaneous contrast is an echocardio-
making. Of all ultrasonic techniques, intravascular graphic indicator (Table 10, 11) of reduced or absent
ultrasound has gained the highest accuracy[100,101,121], flow in the false lumen[6,94]. Similar signs of reduced flow
eliminating the blind spot in the ascending aorta or in can be detected by MRI[136–138].

Eur Heart J, Vol. 22, issue 18, September 2001

1656 Task Force Report

Non-communicating aortic dissections should be dif- epi- and pericardium are indicative of pericardial
ferentiated from intramural haematomas. Intramural effusion. An effusion as little as 30 ml can be detected
haematomas (class 2 aortic dissection) are more local- by echocardiography, but CT and MRI are sensitive
ized and restricted to one or two aortic segments; they methods as well. Fluid around the aorta is a sign of
are frequently characterized by multiple wall layers with ongoing penetration or perforation, not uncommonly
shearing of the different components during pulsation. A combined with intramural haemorrhage[6]. Fluid within
class 2 dissection can progress to a class 1 dissection. the pleural space can be detected by echocardiography,
Non-communicating aortic dissection in a wider sense is CT and MRI. It is usually left sided.
a class 1 dissection but without an entry tear and flow Mediastinal haematomas increase the distance be-
into the false lumen and should be differentiated, be- tween aorta and oesophagus as well as left atrium. A
cause these lesions have a better prognosis than class 2 distance of more than 1 cm is a clear indicator of
dissections. mediastinal haematoma, which might even compress the
If communication is present, the entry points need to left atrium. This can be detected by TEE, CT and MRI.
be located and described with reference to the entire Fluid around the aorta may be a sign of ongoing
dissected segment of the aorta. Antegrade dissection penetration, eventually resulting in rupture. It is import-
is present when the tear is proximal to the distal end of ant to identify these signs of emergency as they are
the dissection. When the tear is located distally to the associated with a mortality of greater than 50%[6]. Some
proximal end of the dissection, retrograde progression deaths may even occur during additional diagnostic
is present. The new imaging techniques allow differen- procedures which delay surgical intervention[6].
tiation of these different types of dissection with high
accuracy. Retrograde dissection with involvement of the
Assessing flow in the false and true lumen
ascending aorta and presence of a tear at the aortic
It is important to differentiate between true and false
isthmus is found in up to 20% of type A (type I)
lumen (Table 11). The true lumen is usually compressed
patients[6]. That means, a retrograde dissection type B
by the false lumen, and demonstrates systolic expansion
(type III) can extend to the ascending aorta and evolve
and systolic forward flow. It is close to the inner
to a type I or type A dissection.
curvature of the aortic arch. Spontaneous echocardio-
When class 1 or 2 dissections (Fig. 5) are excluded and
graphic contrast as a sign of slow flow and thrombus
typical symptoms are present, other forms of dissection,
formation is rare. The false lumen exhibits systolic
such as class 3 and 4 should be considered. Plaque
compression. It is located next to the outer portion of
ulceration following plaque rupture is typically visual-
the aorta and signs of slow flow are regularly described;
ized by TEE, CT or MRI[105–110,135,139–141]. It has to be
at least in some part of the false lumen, if not in its
taken into account that multiple lesions are often
entirety. Thrombus may be present[3,6,94].
present. Each one has to be carefully checked for signs
The true lumen expands during systole and collapses
of penetration or rupture[139].
during diastole because the pressure changes. The col-
While the patient’s history may already point toward
lapse can be complete, giving rise to ischaemia of
the presence of class 5 dissection, class 4 dissection may
tissues/organs supplied by side branches. Flow and
be best visualized by aortography, where it can be seen
pulsation can be attenuated in the true lumen when there
as an eccentric, discrete wall bulging[141]. Class 5 dissec-
is no abdominal reentry.
tion resulting from iatrogenic injury will usually be
If the false lumen is completely thrombosed it can be
evident when a false transit of the catheter is demon-
helpful to analyse the aortic structure in different scan
strated on the aortic contrast injection. Class 5 trau-
fields, and to look for central displacement of calcifi-
matic aortic dissections are best visualized by immediate
cation[2,3,90,121,137]. Further differentiation can be accom-
TEE in the emergency room. Nowadays newer emer-
plished with colour flow and pulsed Doppler[6,94]. Flow
gency rooms may be equipped with mobile CT scanners
in the false lumen is delayed, absent or even reversed[94].
in order to facilitate the use of CT without having to
In addition, communicating dissection intimal flaps
transport the patient.
show stronger pulsation than non-communicating dis-
section. The extent of flow visualization in the false
Indicators of emergency lumen depends on the degree of communication. In
patients with no or reduced communication between the
Clinically aortic dissection will often present as a two-
true and false lumen, imaging shows absent or only
step process. After a first event which is associated with
reduced flow in the false lumen. If by TEE no flow is
severe pain and pulse loss, the bleeding stops. The
present, communication can be ruled out. Retrograde
second event sets in when the pressure exceeds a critical
dissection can still be present, with communication
limit and rupture occurs, either into the pericardium
occurring at a site much more distal, because no flow
with cardiac tamponade or into the pleural space or
reaches the imaged part of the aorta[94].
Fluid extravasation into the pericardium, pleural
space and/or mediastinum are indicators of urgency. Severity and aetiology of aortic regurgitation
These findings are frequently described in cases of An elevated pressure amplitude as well as a diastolic
sudden death in aortic dissection[6,142]. Separation of murmur are often the presenting clinical signs of aortic

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1657

dissection. Increased left ventricular contraction with or Additional information

without dilatation can be regarded as an indirect sign
of aortic insufficiency. Colour flow Doppler has a Supra aortic — arch involvement
high sensitivity and specificity for detecting aortic To plan acute operative interventions, knowledge of the
regurgitation. In addition, aortic regurgitation can be involvement of aortic side branches is not essential as
recognized and graded by cine MRI but not by CT. the ascending aorta will be replaced with or without
Aortic regurgitation can be graded angiographically. valve replacement, irrespective of the extension of the
The aetiology of the regurgitation and the diameter of dissection into side branches[87].
the aortic ring are important to the surgeon, as a Side branches of the aortic arch — the carotid arteries
decision for aortic value replacement or resuspension in particular — are best depicted angiographically, but
has to be made. TEE is currently the best technique to can also be shown on duplex sonography, helical-CT
assess the morphology and function of the valve and and MRI. Using TEE, the innominate artery can be
surrounding structures[77]. visualized in 70% and the left carotid artery in 30% of
cases. Intravascular ultrasound with a 10 MHz trans-
Signs of myocardial ischaemia ducer reliably visualizes all aortic side branches[100,121].
When chest pain is present, it will not be possible to
differentiate between myocardial ischaemia and/or aor- Involvement of abdominal aortic side branches
tic dissection. The ECG will show ST segment elev- Multiorgan failure is a major cause of death after
ation and typical signs of acute transmural myocardial medical or surgical therapy[6,86–88,114]. Flow in abdomi-
infarction when an ostium of the coronary arteries is nal arteries is very often impaired. Sonography is of
blocked. These ECG signs may be so typical that limited value because the imaging quality is often not
thrombolytic therapy is started[123]. Signs of previous good enough for decision making.
myocardial infarction have to be taken into account in Aortography and intravascular ultrasound reveal two
order to be aware of coronary artery disease. Wall pathophysiological mechanism of branch vessel compro-
motion abnormalities detected by echocardiography or mise associated with aortic dissection:
MRI are indicative of reduced myocardial perfusion. (a) static narrowing of a branch artery and
Another sign of ischaemia may be ST-segment depres- (b) dynamic narrowing of a branch artery.
sion indicating non-transmural infarction or coronary Static narrowing occurs when the line of dissection
insufficiency secondary to deteriorating haemo- intersects the vessel origin and the aortic haematoma has
dynamics in coronary artery disease, flaps blocking the propagated into the vessel wall stenosing the side branch
coronary ostium or collapse of the true lumen during lumen. In dynamic obstruction the line of dissection
diastole[143]. spares the vessel but the dissection flap is positioned
Transoesophageal echocardiography can visualize the across the vessel origin like a curtain, or in other words,
ostium of both arteries and image the first 2–3 cm of the the flap spares the branch vessel wall but collapses
left and 1–2 cm of the right coronary artery. Multislice across the branch vessel origin covering it like a curtain.
CT and MRI may visualize the proximal coronary Both mechanisms may be present in a given patient at
arteries in emergency situations even better. the same time at different levels. Angiography may be
Currently only coronary angiography can reliably necessary to identify these mechanisms, as interpretation
determine whether additional coronary artery disease is of MRI or CT images may be difficult. Involvement of
present in patients with aortic dissection. In stable side branches of the aorta such as the coeliac artery,
patients, particularly those with aortic type B (type III) mesenteric or renal arteries can be detected with intra-
dissection, coronary angiography can be performed vascular ultrasound[100,121].
safely and represents a part of the staging in the chronic
phase of the disease[144,145]. Iliac and femoral artery involvement
In aortic dissection without a distal tear (reentry) the
aorta may become totally obstructed as the true lumen is
Summary compressed by the false lumen. The extent of the dis-
section can be visualized by CT or MRI. The true lumen
Essential information in involving acute aortic
is usually located anteriorly and the false lumen pos-
teriorly. Angiography is necessary in order to visualize
+ Confirmation of diagnosis
the full anatomical situation including collateral flow. In
+ Tear localization
the future, MRI angiography may replace conventional
+ Extent of aortic dissection
+ Classification of aortic dissection
+ Indicators of emergency
Additional information not immediately necessary Laboratory testing
+ Arch vessel and side branch involvement Laboratory testing plays a minor role when assessing
+ No laboratory tests except for routine parameter acute aortic dissection, but it is useful to exclude other
assessment diseases. Often signs of inflammation with elevation of
C-reactive protein are found.

Eur Heart J, Vol. 22, issue 18, September 2001

1658 Task Force Report

Table 12 Diagnostic imaging in acute aortic dissection

Recommendation Class I IIa IIb III Level of evidence

1. Transthoracic echocardiography followed by transoesophageal echocardiography + C

2. Computed tomography + C
+ if detection of tears is crucial + C
3. Contrast angiography
+ to define anatomy in visceral malperfusion and to guide percutaneous interventions + C
+ in stable patients + C
+ routine preoperative coronary angiography + C
+ in haemodynamically unstable patients + C
4. Magnetic resonance imaging + C
+ in haemodynamically unstable patients + C
5. Intravascular ultrasound + C
+ to guide percutaneous interventions + C

Beyond the acute situation, genetic testing of patients (2) the identification of a mutation in the COL3A1
and relatives may be indicated. The identification of the gene, or
FBN-1 gene leads to the development of two types of (3) linkage analysis with intragenic polymorphic
diagnostic tests: genetic family studies and mutation markers[32]. The latter is difficult since mutations are
identification. private and widely distributed throughout this large
(1) Family studies can be performed with specific and fragmented gene[32]. Furthermore, it must be
FBN-1 polymorphic markers to identify the noted that mutations within this gene are not specific
mutation-bearing haplotype[146,147]. These studies since they are also found in patients with EDS types
are only reliable in families with several affected II (classical type mitis) and III (hypermobility type
individuals (at least four) as the involvement of a also associated with mutations in the COL5A1 or
FBN-1 mutation (and not that of another gene) COL5A2 genes) which also display an autosomal
must be clearly demonstrated. Most families do not dominant mode of inheritance. No phenotype–
meet this requirement. Furthermore, the method is genotype correlations have been identified yet.
inappropriate in sporadic cases. In practice, these The mutation therefore does not predict the disease
instances represent over 40% of the cases referred for type, course and severity. Finally, genetic hetero-
biological diagnosis. geneity has been reported[15]: a few patients with
(2) The second molecular test is mutation identification. very similar recessively inherited clinical presen-
This test should only be performed after the protein tation, have apparently normal collagen III
analysis or the previously mentioned family study metabolism[19].
has conclusively shown the presence of a FBN-1 In annuloaortic ectasia genetic heterogeneity and
gene defect. Mutation identification is very costly current technical shortcomings make genetic analysis
and time consuming. In fact, there is no quick and difficult. Only two of the genes involved have been
100% reliable method to investigate a large gene, identified. Both are very large and there is no evidence to
knowing that almost each family has its own specific suggest a clustering of mutations within specific regions
defect and that the mutations are essentially point of these genes associated with dissecting aortic aneu-
mutations. Finally, this very costly analysis may rysms. It is therefore unreasonable to screen these genes
fail to identify a mutation since only the coding systematically. However, since antibodies are available
sequence and closely surrounding regions are against collagen III and fibrillin-1, structurally or
investigated. metabolically abnormal proteins can be demonstrated
(3) In all other instances and until better molecular tools in fibroblast cell cultures. These tests cannot be
are available, mutation identification cannot be per- recommended as routine measures.
formed on a systematic basis. However, in a few
cases where the family mutation had been identified,
it is possible to perform pre-natal diagnosis on
chronic villus samples or offer diagnostic evaluation Imaging modalities
in children of affected subjects before symptoms set
in[148,149]. There are also recent reports of preimplan- Different direct and indirect methods as well as in-
tation genetic diagnosis of Marfan’s syndrome[150]. vasive and non-invasive techniques can be employed to
In Ehlers-Danlos syndrome laboratory diagnosis is diagnose aortic dissection (Tables 12, 13). The different
based on: imaging modalities are briefly described, taking into
(1) demonstration of structurally abnormal collagen account technical considerations, specific diagnostic
type III by fibroblasts, criteria, and the accuracy of the methods (Table 14).

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1659

Table 13 Imaging in chronic aortic dissection

Recommendation Class I IIa IIb III Level of evidence

1. Magnetic resonance imaging + C

2. Transthoracic echocardiography followed by transoesophageal echocardiography + C
3. Computed tomography + C
4. Conventional angiography
+ to guide percutaneous interventions + C
+ pre-operative diagnosis in selected patients + C
+ for complete staging of the disease + C
5. Intravascular ultrasound
+ to guide percutaneous interventions + C

Transthoracic/transoesophageal dissection membrane[94]. The number of tears is re-

corded and the location as wall as the distance from the
echocardiography (TTE/TEE) teeth to the tip of the probe is documented.
Technical considerations The differentiation in the true from the false lumen is
The aorta and the major aortic side branches can be based on M-mode, two-dimensional, and Doppler
studied using different scanning fields. It is important to echocardiographic signs[155]. Criteria for identifying the
true lumen are systolic expansion and diastolic collapse,
use all scanning planes in order to provide complete
the absence or low intensity of spontaneous echocardio-
information about the type and extension of aortic
graphic contrast, systolic jets directed away from the
dissection. M-mode and two-dimensional echocardiog-
lumen, and systolic forward flow, whereas criteria for
raphy are taken in standard cross-sectional planes: par-
the false lumen are diastolic diameter increase, spon-
asternal, apical, subcostal scan fields. The ascending
taneous echocardiographic contrast, reversed, delayed,
aorta is visualized in left parasternal projections. In
or absent flow and thrombus formation[6,155]. Flow
aortic ectasia the right parasternal view and the apical
signals within the false lumen represent signs of com-
view are useful. The aortic arch is best visualized via the
munication, whereas the absence of flow signals in
suprasternal approach. Orthogonal and longitudinal
multiple cross-sections means no communication. If the
scan planes can provide information concerning exten-
only communication is found distal to the beginning of
sion of dissection into the innominate artery, left com-
the dissection, retrograde dissection can be assumed,
mon carotid or left subclavian artery. The descending
which can be further differentiated into retrograde
aorta can occasionally be vizualized in the left para-
dissection with or without involvement of the ascending
sternal cross-sectional image and via specialized para-
spinal scan fields obtained by imaging the patient
A thrombus is diagnosed when a mass separate
through the back in the right decubitus position or by
from the intimal flap and the aortic wall is imaged in
using abdominal scan planes[151–152].
Transoesophageal echocardiography is performed the free space of the false or rarely the true lumen[6].
Because thrombus formation depends on flow velocity,
with 3·5 and 7·0 MHz transducers which consist of 32,
it may be graded to provide an estimate of the degree of
64 or more elements mounted on the distal end of
conventional 9 to 15 mm gastroscopes (echoscope).
Echo-free spaces resulting from the presence of free
Single plane, biplane and multiplane transoesophageal
fluid around the aorta are judged to be signs of pen-
echocardiographic probes are available. These new
etration due to periaortic haematoma[6]. Additional
modalities allow visualization of the aorta in any given
mediastinal haematoma is assumed when the distance
angle and therefore better special orientation[153]. On the
basis of multiple tomographic cross-sectional images, from the oesophagus to the left atrium or the aorta
3-D reconstruction of the aorta can be performed[154]. is increased (>1 cm) and pleural effusion is found.
Pericardial effusion is considered to exist when an echo-
Echocardiographic criteria of aortic dissection free space between the epicardium and pericardium is
The diagnosis of aortic dissection is confirmed when two present[6].
Aortic regurgitation is diagnosed when disturbed
lumina separated by an intimal flap can be visualized
diastolic flow signals are detected in the left ventricular
within the aorta. Positive criteria are complete obstruc-
outflow tract. Grading is performed by taking Doppler
tion of a false lumen, central displacement of intimal
and colour Doppler echocardiographic criteria into
calcification, separation of intimal layers from the
thrombus, and shearing of different wall layers during
aortic pulsation[6]. A tear is defined as a disruption of the
flap continuity with fluttering of the ruptured intimal Accuracy of TTE/TEE
borders[3,6,94]. Smaller intimal tears can be detected The diagnosis of aortic dissection by standard transtho-
by colour Doppler, registering jets transversing the racic M-mode and two-dimensional echocardiography

Eur Heart J, Vol. 22, issue 18, September 2001

1660 Task Force Report

is based on detecting intimal flaps in the aorta. Sensitiv- Computed tomography

ity and specificity of transthoracic echocardiography
range from 77% to 80% and 93% to 96%, respectively, Since its introduction, helical CT has dramatically im-
for the involvement of the ascending aorta[151,152,157]. proved CT diagnostics because it minimizes motion
However, in previous series, transthoracic echocardiog- artifacts and eliminates respiratory misregistration.
raphy was successful in detecting a distal dissection of With conventional CT, each cycle of the X-ray tube
the thoracic aorta in only 70% of the patients[157]. generates data which are used to reconstruct transaxial
The value of transthoracic echocardiography is limited images. With helical CT, patient translation and X-ray
in patients with abnormal chest wall configuration, exposure are simultaneous. This technique provides a
narrow intercostal spaces, obesity, pulmonary emphy- data set acquired during a single breathhold. These data
sema, and in patients on mechanical ventilation. These can be used to reconstruct 2-D and 3-D images in any
limitations prevent adequate decision-making, but plane. In fact, CT is currently the most commonly
have been overcome by transoesophageal echo- used imaging modality in patients with suspected aortic
cardiography[6]. dissection[130].
Only experienced examiners should interpret echo-
cardiographic studies. The European cooperative study Technique of computed tomography
group[3] showed that sensitivity of TTE and single plane, Imaging results depend on many factors, including
occasionally biplane, but not multiplane TEE reaches X-ray beam collimation and table feed. The choice of
99%, specificity 89% and positive predictive accuracy the reconstruction interval is critically important to the
and negative predictive accuracy 89% and 99%, respect- success of the imaging procedure, and its settings are
ively. This was confirmed by others[158]. When the important in terms of spatial resolution. Reconstruction
analysis was limited to patients who underwent surgery algorithms are highly critical to achieve optimal aortic
or autopsy, the sensitivity of TEE was only 89%, the imaging. Once transaxial images have been recon-
specificity 88%, the positive predictive accuracy 97% and structed, high quality 2-D reformations may be gener-
the negative predictive accuracy 93%[3]. ated in desired planes (Multiplanar Reformation (MPR)
A problem exists in visualizing small circumscript Images). Maximum intensity projection images (MIPs)
dissected segments within the distal part of the ascend- are generated by projecting imaginary X-rays through
ing aorta and the anterior portion of the aortic arch, the 3-D matrix of interpolated images and mapping the
which is known as the ‘blind spot’[3]. This problem maximum attenuation values along each ray to a gray
is caused by interposition of the trachea and the left scale image. This technique provides ‘angiogram-like
main stem bronchus between the oesophagus and the images’. Shaded surface display (SSD) images are
aorta. generated after applying an arbitrary user-selected
Artifacts due to reverberation within the lumen of the threshold. Voxels in the matrix of interpolated images
ascending aorta can be observed. These artifacts may are displayed as 3-D images, with depth perception
present a problem to non-experienced observers[3] and added by shading from a virtual light source.
may be the cause of the low sensitivity in one of the The basic setting comprises 3 mm collimation and
previous reports[159]. 6 mm . s 1 table feed[137,138,160]. The start delay is
By two-dimensional transoesophageal echocardiogra- determined by specific software which detects the con-
phy, the intimal tear can be identified in 61% of patients. trast medium in a region of interest. 120 ml of low
Doppler flow analysis has shown that not only uni- osmolar contrast medium is injected at a rate of
directional but also bi-directional flow occurs between 1–3 ml . s 1 with a power injector. Images are recon-
the two lumina. Bi-directional flow is present in 75% of structed at 2 mm intervals with overlap[137,138]. MPRs
patients. By continuous wave Doppler a pressure gradi- are generated in sagittal, coronal, oblique sagittal pro-
ent between the true and false lumen can be measured; it jections. MIP and SSD images are produced as an
tends to be within the range of 10 to 25 mmHg[94]. option. The first acquisition covers the thoracic aorta, a
second acquisition with the same injection technique is
necessary to examine the abdominal aorta and iliac
Summary arteries.

Transoesophageal echocardiography in addition Diagnostic CT criteria for aortic dissection

to transthoracic echocardiography can be used for The diagnosis is based on the demonstration of an
decision making in the emergency room or even intimal flap which separates the true from the false
operating theatre in acute aortic dissection with channel. The flap is identified as a low attenuation linear
high accuracy. Pitfalls have to be taken into ac- structure in the aortic lumen[137,160]. Secondary findings
count. The high resolution enables the diagnosis include internal displacement of intimal calcifications,
also of intramural haematoma, plaque ulcer- delayed enhancement of the false lumen and aortic
ation, as well as traumatic aortic injury. When more widening. MIP and MPR are useful both for making the
spatial resolution is necessary, CT or MRI are used initial diagnosis and for assessing the extent of the
in addition. dissection. The technique can depict involvement of
visceral as well as the iliac arteries.

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1661

Reported limitations to the interpretation of CT aor- imaging time is comparable to that required for per-
tography are due to two artifacts: venous streaks and forming a transoesophageal echocardiographic study.
aortic motion artifacts. Venous streaks are easily ident- Even if sensitivity and specificity values are based on
ified because their orientation varies from slice to slice the experience gained with conventional MR-imaging
and extends beyond the limits of the aortic wall. Aortic sequences[160,161], image quality is usually even better
motion artifacts are related to motion of the aortic wall, with breathhold imaging, and at least the same diagnos-
and particularly the intimal flap in the interval between tic accuracy can be expected. New real-time MR imag-
the end of the diastole and the end of the systole. The ing sequences, which are available on the most advanced
use of a 180 linear-interpolation algorithm will clearly scanners, should further facilitate the diagnosis of aortic
reduce or remove these artifacts. Mural thrombi in a dissection in unstable patients[162].
fusiform aneurysm can be mistaken for aortic dissection. Another new MRI tool to image aortic dissection is
Structures or masses around the aorta may also make a three-dimensional contrast enhanced MR aortography.
diagnosis difficult. Images are similar to invasive aortography but the
field of view is larger. Initial experience suggests that
Accuracy of CT the diagnosis of aortic dissection can be made
Sensitivities of 83%–94% and specificities of 87%–100% reliably[163,164]. Thus, a combination of MR aortography
have been reported in the early 1990s in large prospec- with cross-sectional MR images may be ideally suited
tive studies on the evaluation of aortic dissections with to get both an overview of aortic anatomy (important
conventional incremental CT[3,137]. The benefits of heli- for surgical planning) and details of the dissecting
cal CT compared to incremental CT are well established membrane and the aortic walls.
and include shorter examination times and the potential
for better evaluation of the aorta, as all images are
Diagnostic MR criteria for aortic dissection
obtained during optimal contrast enhancement[137].
MRI clearly demonstrates the extent of the disease and
Artifacts are significantly reduced. The average
depicts the distal ascending aorta and the aortic arch in
sensitivity is better than 95%[137,138]. Sensitivity and
more detail than even transoesophageal echocardiogra-
specificity for diagnosing arch vessel involvement are
phy[165]. The localization of entry and reentry is nearly
93% and 98% respectively, with an overall accuracy of
as accurate as with transoesophageal echocardiography,
the sensitivity approaches 90%[165]. Accordingly, classi-
fication of the disease into proximal and distal aortic
Summary dissection which is crucial for selecting the appropriate
management, can be easily accomplished with MRI.
CT is the technique used most often in patients with Adverse signs such as the presence of pericardial effusion
suspected aortic dissection. or aortic regurgitation can be assessed accurately[160,166].
The sensitivity is greater than 90%, specificity Flow in the false and true lumen can be quantified using
greater than 85%. The extent, localization and side phase contrast cine magnetic resonance imaging or by
branch involvement of aortic dissection can be tagging techniques[167,168]. With state-of-the-art MRI,
assessed, signs of emergency detected. Limitations the proximal coronary arteries and their involvement in
are related to diagnosis of aortic regurgitation, tear the dissecting process can be clearly delineated[169].
localization as well as detection of intimal tears and However, no direct comparison between imaging tech-
subtle /discrete aortic dissection (class 3). niques regarding depiction of coronary involvement has
been published yet.

Magnetic resonance imaging Accuracy of MRI

Despite the accuracy of MRI, certain pitfalls and
Although MRI is both highly sensitive and specific in artifacts on MRI images need to be recognized and
diagnosing aortic dissection[137,138,161], the technique is experience in reading MRI images of aortic dissection
often not available on an emergency basis and exami- is essential[170]. Some kind of artifact may occur in up
nation of haemodynamically unstable patients may be to 64% of patients but most of these artifacts are only
difficult. However, in centres with experience in moni- seen in one section but not in the neighbouring ones.
toring cardiac patients and even haemodynamically un- This observation facilitates the recognition of an arti-
stable patients on mechanical ventilation, MRI can be fact and distinguishes it from a pathological finding.
performed without complications[5]. Use of another imaging technique to make this distinc-
tion was required in only 2% of MR examinations.
Technique of MRI Awareness of the existence of artifacts, knowledge of
Whereas conventional spin-echo MRI and cine MRI normal anatomy, the use of axial images in all cases
require substantial imaging time to cover the entire plus the addition of images in other planes as needed,
aorta from the arch vessels down to the aortic bifurca- rotation of phase and frequency gradients as needed,
tion, new rapid scanning techniques permit image acqui- and clinical correlation may avoid misinterpretation in
sition at multiple levels within a single breathhold. Thus, nearly all cases.

Eur Heart J, Vol. 22, issue 18, September 2001

1662 Task Force Report

Magnetic resonance imaging permits detection of ogists. Rarely, angulated views are required to depict the
acute and subacute aortic intramural haemor- ostia of some abdominal side-branches. Alternatively,
rhages[90,171]. Typical features of intramural haemor- intravenous aortography with digital subtraction may
rhage include a thickened wall (>7 mm) with a smooth be performed by injecting contrast material into the
surface which may contain areas of high signal intensity. antecubital vein or directly into the right atrium or
The high signal intensity is the result of methemoglobin superior vena cava[175]. This technique is less invasive
formation which occurs after several days and persists and requires smaller amounts of contrast media but
for several months, although it may be absent in the it usually provides lower resolution images than
acute phase[171]. Because intramural haemorrhage of the conventional angiography.
thoracic aorta may be associated with true dissection of
the abdominal aorta, the latter should also be evaluated. Diagnostic aortography: criteria for aortic dissection
Magnetic resonance imaging could not detect subtle The angiographic diagnosis of aortic dissection is based
degrees of dissection — in a small series of cases neither upon ‘direct’ (diagnostic) angiographic signs, such as the
did CT or TOE[89]. But plaque rupture can be visualized visualization of the intimal flap (negative, often mobile,
with high accuracy, as well as traumatic iatrogenic linear image) or the recognition of two separate lumens,
dissection. or ‘indirect’ (suggestive) signs, including aortic lumen
contour irregularities, rigidity or compression, branch
vessels abnormalities, thickening of the aortic walls and
Summary aortic regurgitation[157]. Aortography is able to localize
MRI has the highest accuracy and sensitivity as well the site of origin of the dissection[175]. The true lumen is
as specificity (nearly 100%) for detection of all typically compressed and tends to adopt a spiral shape.
forms of dissection (class 1, 2 and 4, 5) except Injections in the false lumen are characterized by the
subtle/discrete forms (class 3). Distribution and absence of branch vessels or the characteristic sinus of
availability is limited particularly in emergency situ- Valsalva configuration and late filling or staining with
ations. Most often MRI is used in stable haemo- contrast[176]. Contrast aortography accurately identifies
dynamic conditions and chronic aortic dissection branch vessel involvement[176]. It is mandatory to rule
for follow-up. MRI provides excellent visualization out this complication in patients with neurological
of tear localization, aortic regurgitation, side branch symptoms, acute renal failure, hypertensive crisis or
involvement and complications. mesenteric/limb ischaemia. Peripheral pulse deficits can
provide important diagnostic clues. In particular, angi-
ography is an excellent technique to define renal or
mesenteric compromise[177]. The occurrence of associ-
Aortography ated aortic regurgitation and its severity may be readily
recognized during aortography. However, this technique
Retrograde aortography was the first accurate diagnos- has recently been replaced by other new imaging modali-
tic tool to assess patients with suspected aortic dissec- ties with respect to its ability to evaluate the precise
tion. The diagnosis of aortic dissection was first reported mechanism of aortic regurgitation. In some patients,
by Robb and Steinberg in 1939 and it became routine in however, angiography may reveal widening of the aortic
the 1960s[172,173]. Thereafter, aortography was consid- root, displacement of a valve cusps or even prolapse of
ered for several decades as the diagnostic standard for an intimal flap into the left ventricle as the underlying
the evaluation of aortic dissection[174]. However, because mechanism[178,179]. Aortography may also demonstrate
other accurate methods for the antemortem diag- aortic wall rupture into the pericardial cavity, right
nosis of aortic dissection were not yet available, the low atrium, left atrium, right ventricle and pulmonary
sensitivity of angiography was accepted. artery[179].

Technique of aortography Accuracy of aortography

To visualize the signs of aortic dissection, injections of The specificity of aortography for diagnosing aortic
adequate amounts of contrast media (40–50 ml at 20– dissection is better than 95% but its sensitivity may be
25 ml . s 1) at different levels and using different projec- lower than that of other techniques, especially in atypi-
tions are usually required, to best define the thoracic cal forms of aortic dissection[178]. In the European
aortic anatomy in each individual patient[175,176]. The cooperative study, the sensitivity and specificity of aor-
transit of the contrast material along the aorta can be tography for the diagnosis of aortic dissection was
followed. Special care is to be taken to fully opacify the 88%[3]. False-negative aortograms are mainly the result
proximal aspect of the brachiocephalic trunk and to use of the inability of the technique to differentiate the two
appropriate projections[176]. For abdominal aortogra- classic lumens within the aorta[3,6,153,180,181]. Aortograms
phy, a single injection of 40 ml of contrast agent at a rate yielded false-negative results in 15 of 65 consecutive
of 20 ml . s 1 is generally adequate for posteroanterior patients with proven aortic dissection (sensitivity
projections, but biplane angiography is required particu- 77%)[182]. The missed diagnosis was due to a completely
larly for the visualization of entry/reentry tears and in thrombosed false lumen or intramural haematoma in 13
order to meet the demands of interventional radiol- patients, and to a large ascending aortic aneurysm with

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1663

nearly equal and simultaneous opacification of the false Coronary angiography

and true lumen[182]. Aortography may be somewhat In some patients delineation of coronary anatomy is
more useful in the diagnosis of aortic dissection with desirable prior to surgical repair. Although new imaging
thrombosis of the false lumen than in typical intramural techniques are gaining an emerging role in the assess-
haematoma, because in the former some degree of lumen ment of coronary ostial involvement by the dissecting
compromise is the rule, whereas the aortic lumen usually flap, coronary angiography remains the gold standard in
remains unaffected in the latter[153]. Nevertheless, despite the evaluation of the whole coronary tree[144,145]. This is
some limitations, angiography remains a widely avail- important because chronic coronary atherosclerotic dis-
able technique in most centres, and many cardiac sur- ease (present in 25% of patients) — although not related
geons feel comfortable with the information it provides. to the process of aortic dissection — may worsen the
This is mostly the consequence of the vast experience surgical outcome. This is a strong argument used by
with this technique. some authors to recommend coronary angiography for
Aortic intramural haematoma (class 2 dissection) has all stable patients. However, whether or not selective
been considered the principal reason for false-negative coronary angiograms should be performed in patients
findings on aortography. A faint shadow corresponding being considered for surgical repair remains indeter-
to the vascular silhouette may appear well separated from mined[145]. Mortality after surgery for aortic dissection
the aortic lumen and this pattern may be indicative of an does not seem to be related to myocardial ischaemia
intramural haematoma. Straightening of the lumen, mild and, therefore, it is unlikely that systematic coronary
luminal narrowing, or irregularities may give some diag- angiography prior to surgical repair can influence out-
nostic clues for a subtle class 3 aortic dissection. Multiple come. It should be left up to the clinical judgment of the
views of the ascending aorta on aortography may provide physician and surgeon whether coronary angiography is
further diagnostic information[89,104,182]. In patients with to be performed.
suspected aortic dissection based on the clinical history,
aortography should be performed when non-invasive
techniques are negative. Summary
In class 4 aortic dissection, penetrating atherosclerotic
ulcers of the distal descending aorta can be diagnosed Aortography is highly valuable to diagnose classical
with angiography, but biplane angiography has to be aortic dissection, but limitations are obvious in
used[105,106]. Penetration surpassing the intima may lead dissection subtypes such as non-communicating
to medial haematoma, penetration to the media may aortic dissection and intramural haematoma and
cause pseudoaneurysm and penetration disrupting the haemorrhage formation (class 2) as well as plaque
adventitia results in aortic rupture; all these signs may be rupture (class 4). Aortography is the standard tech-
detected by angiography[106]. nique for guiding interventions in aortic dissection.
Limitations of aortography
Some limitations of this technique should be recognized.
It is invasive and therefore has an inherent risk. The Intravascular ultrasound
advancement of catheters should be performed with care
and only by experienced angiographers. Forceful push-
ing of the catheter or the guidewire should be strongly Technique of intravascular ultrasound
discouraged to avoid injury, particularly if the catheter To perform an intravascular ultrasound (IVUS) exami-
is located within the false lumen. Pressure measurements nation, disposable catheters are advanced under fluor-
and manual injections of contrast media may be helpful oscopy over conventional guidewires with/without
to differentiate between the true and false lumen. Once guiding catheters. The procedure can be performed
the correct position of the catheter is demonstrated safely in less than 10 min[100,101]. Because of the well-
catheter exchanges should be performed using long known trade-off between frequency and penetration,
exchange wires. In addition, this technique requires the transducers with <20 MHz are preferred, but such
administration of potentially nephrotoxic radiopaque transducers cannot be advanced via guiding catheters
contrast media and ionizing radiation. Furthermore, the (6–8F). The size of 10 MHz transducers reaches 8·2F
intimal flap as well as the distal end of the dissection are (3·3 mm). These transducers are advanced over 0·35 inch
not clearly defined when slow flow is present. It is wires. In regions with aneurysmal dilation the whole
important to emphasize that aortic wall thickness can- aorta cannot be displayed from a single position, when
not be accurately visualized. Aortography may under- 20 or 30 MHz transducers are used. This has been
estimate the luminal size in the presence of non-opacified overcome by 10 MHz transducers. It is difficult to align
thrombus formation[182]. In critically ill patients the time the catheter coaxially within the lumen of the aortic
required for assembling the angiographic team, bringing arch. Prototype flexible catheters which can maintain a
the patient to the angiographic suite and the duration of pre-selected curvature (steerable) are currently under
the procedure itself may be too long to be justified. This investigation[184]. Catheters have been developed which
should always be taken into account as diagnostic delays allow Doppler, tissue Doppler and 2nd harmonic
are associated with an increased mortality[183]. imaging[185].

Eur Heart J, Vol. 22, issue 18, September 2001

1664 Task Force Report

Table 14 Comparing the diagnostic value of imaging techniques in aortic dissection


Sensitivity ++ ++ +++ ++ +++

Specificity +++ ++ +++ ++ +++
Classification +++ ++ ++ + ++
Tear localization +++  ++ + +
Aortic regurgitation +++  ++ ++ 
Pericardial effusion +++ ++ ++  
Mediastinal haematoma ++ +++ +++  +
Side branch involvement + ++ ++ +++ +++
Coronary artery involvement ++  + +++ ++
X-ray exposure  ++  +++ 
Patient comfort + ++ + + +
Follow-up studies ++ ++ +++  
Intra-operative availability +++   (+) (+)

TTE/TEE=transthoracic/transoesophageal echocardiography.
CT=computed tomography.
MRI=magnetic resonance imaging.
IVUS=intravascular ultrasound.

Diagnostic IVUS criteria for aortic dissection and narrowing the vessel origin versus ostium spared by
The use of intravascular ultrasound (IVUS) has been the dissection but covered by a prolapsing flap) may be
advocated to complement angiographic information in clarified by IVUS[100,101,121]. Precise delineation of the
the diagnosis of patients with aortic dissection[100,121]. entry tears is difficult, however, this may be seen more
During a cardiac catheterization procedure, this tech- frequently in the abdominal aorta than in the thoracic
nique can overcome most of the potential limitations aorta[100]. The lack of Doppler capabilities is still a
and pitfalls of conventional angiography. IVUS directly drawback of the technique. Thrombus formation within
visualizes the vessel wall architecture from inside the the false lumen may be predicted by of the appearance of
aortic lumen. It therefore allows the accurate recog- spontaneous echo-contrast.
nition of aortic wall characteristics and pathology, and Changes in the aortic wall due to haemorrhage into
completes the indirect information of ‘the lumen the media are visible by IVUS because of the accompa-
shadowgram’ depicted by contrast angiographic nying increase in wall thickness[100,101]. IVUS is very
techniques. accurate in displaying the circumferential and longitudi-
nal extent of the haematoma. Aortic haematomas ap-
Accuracy of IVUS pear as crescent-shaped or circumferential thickening of
In patients with classic forms of aortic dissection this the aortic wall[121]. In some segments, an echo-free space
catheter-based imaging tool provides crisp visualization is visualized, yielding atypical image of a layered aortic
of the intimal-medial flap, its movement (pulsatility), its wall[100,101,121]. In other areas, speckled granular reflec-
circumferential and longitudinal extent and the degree of tions are recognized within the aortic wall. The shape of
luminal compromise. This technique appears particu- this intramural haemorrhage may be concentric and
larly well suited to delineate the most distal extent of affect the complete aortic circumference, but it is typi-
abdominal aortic dissections[100,121]. Sensitivities and cally limited to a segment of the aorta. IVUS appears
specificities of close to 100% have been reported[121]. The particularly useful to rule out the presence of pulsatile
shape of the true and false lumen is readily displayed, intimal flaps and deeply penetrating atherosclerotic
whereas false lumen thrombosis is detected with a higher ulcers, when others techniques give inadequate results.
sensitivity and specificity than with transoesophageal In addition, it appears particularly attractive for
echocardiography[121]. IVUS may also help to distin- patients with suspected aortic dissection and a normal
guish the true from the false lumen when it is difficult to aortography[121].
make this distinction. It has been suggested that the
three-layered appearance of the intact normal aortic wall
may be differentiated from the single-layered appearance Surgical and interventional therapy
of the outer wall of the false lumen. In addition, Surgical therapy
cobwebs may be identified in the false lumen in some
patients. Branch involvement appears to be better de- Introduction
fined with IVUS than with transoesophageal echo- The aim of any surgical intervention in type A (type I,
cardiography (blind spot in the ascending aorta and the II) aortic dissection is the prevention of aortic rupture or
anterior portion of the arch, abdominal vessels) or with of the development of pericardial effusion which may
computed tomography[121]. In addition, the precise lead to cardiac tamponade. It is also imperative to
mechanism of vessel compromise (dissection intersecting eliminate aortic regurgitation and to avoid myocardial

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1665

Table 15 Surgical therapy of acute type A (type I and II) aortic dissection

Recommendation Class I IIa IIb III Level of evidence

1. Emergency surgery to avoid tamponade/aortic rupture + C

2. Valve-preserving surgery — tubular graft if normal sized aortic root and no + C
pathological changes of valve cusps
3. Replacement of aorta and aortic valve (composite graft) if ectatic proximal + C
aorta and/or pathological changes of valve/aortic wall
4. Valve-sparing operations with aortic root remodelling for abnormal valves + C
5. Valve preservation and aortic root remodelling in Marfan patients + C

Table 16 Surgical therapy of acute type B (type III) aortic dissection

Recommendation Class I IIa IIb III Level of evidence

1. Medical therapy + C
2. Surgical aortic replacement if signs of persistent or recurrent pain, early + C
expansion, peripheral ischaemic complications, rupture
3. Surgical or endovascular fenestration and stenting if persisting mesenteric, + C
renal or limb ischaemia or neurologic deficits

ischaemia. In type B (type III) dissection it is the main the patient is on extracorporal circulation, which is
goal to prevent aortic rupture. One should always aim to usually established after cannulation of one femoral
resect the intimal tear in class 1 dissection. Whereas in artery and the right atrium, the aorta is mobilized for
aortic dissection limited to the ascending aorta with or visualization of the origin of the innominate artery and
without involvement of the aortic arch, the resection of the aortic root. If the aortic arch is to be replaced,
the entire intimal flap may be possible, a full repair of surgical dissection proceeds along its anterior aspect and
the aortic dissection is rarely reached in type A and type the origins of the arch branches are prepared.
B (type I–III) dissection (Tables 15, 16). Various ap- An acute type A (type I, II) dissection in a previously
proaches to the repair of the acutely dissected aorta have ectatic proximal aorta requires a different approach.
been suggested. This fact sheds light on the remarkable In such instances — this includes most patients with
methodologic variability[186–190]. Marfan’s syndrome — implantation of a composite
graft (aortic valve plus ascending aortic tube graft) is
The proximal aorta in acute type A (type I and II) recommended[192,193]. In the original method described
aortic dissection by Bentall and De Bono, the coronary ostia remain in
Two key questions need to be answered prior to deciding continuity with the ‘old’ aorta and are anastomosed
on the most appropriate technique for repairing an acute directly to the ascending portion of the graft after valve
type A (type I, II) dissection: what is the size of the implantation[194]. If the coronary ostia are close to the
aortic root and what is the condition of the aortic valve? aortic annulus and if a stiffened aortic wall creates
If the ascending aortic and aortic root diameters are tension on the ostia when they are relocated to the graft,
normal without downstream displacement of the cor- they may be excised in button form before being anas-
onary ostia, and with no commissural detachment of the tomosed[195]. Implantation of allografts and xenografts
aortic valve leaflets or other acute or chronic pathologi- should be restricted to elderly patients or special other
cal changes of the leaflets, a tubular graft is usually indications since late postoperative degeneration may
anastomosed to the sinotubular ridge (Table 15). When- require reoperation on the aortic root. More recently,
ever one or more commissures are detached, the valve valve sparing operations and/or aortic root remodelling
needs to be resuspended prior to graft insertion. If valve have been suggested even in the emergency situation of
reconstruction appears unsafe, or if obvious congenital an acute type A (type I, II) dissection[196,197]. As these
or acquired abnormalities are present, it is generally procedures are more complicated and time consuming
better to replace the valve before a supracommissural than composite grafting, they should only be performed
graft is inserted. However, the repair of bicuspid valves by surgeons who have broad experience with such
has been reported[191]. procedures in elective cases.
The standard approach to the ascending aorta and The distal connection of the tube graft is made to the
transverse aortic arch in aortic dissection type A (type I, uninvolved ascending aorta in those relatively rare cases
II) is through median sternotomy. The pericardial inci- of limited type A (type II) dissection. In all other
sion is started in the midline inferiorly in order to avoid patients, replacement is carried to the junction of the
the dissected and therefore friable ascending aorta. Once ascending aorta and arch or beyond that level.

Eur Heart J, Vol. 22, issue 18, September 2001

1666 Task Force Report

Technical considerations for the management of the operations mentioned above are another option. They
dissected non-ectatic aortic root first address the con- may be indicated in root ectasia. A basic consideration
dition of the aortic valve commissures (Table 15, 16) as to be applied to these procedures is that aortic incom-
well as the presence and extent of the dissection in petence commonly results from dilatation of the sinu-
relation to the coronary ostia. If the dissection has tubular ridge rather than the annulus[200]. The aorta is
reached either ostium without disrupting the coronary fully divided 5 mm above the valve commissures and the
vessel, the ostium can usually be preserved. An ostium leaflets are examined for symmetry and absence of
completely surrounded by dissected aortic wall may be organic disease[196]. In David’s techniques the coronary
excised in button form. The dissected layers around the sinuses and the coronary ostia are excised leaving the
ostium are conjoined using tissue adhesive and over- valve cusps and their insertion lines intact. As the
and-over suturing before the anastomosis to a tube graft next step a mattress suture is passed through the apex
is accomplished. Bypass grafting of coronary arteries of each commissure before transmural mattress sutures
using saphenous vein segments is limited to those in- are placed through the aortic annulus. The annular
stances where a small torn ostium with irreparable sutures are then passed through the cardiac end of a
damage precludes secure reconstruction. prosthetic graft and the aortic valve remnants are drawn
The creation of a firm and leak proof seat of the into the graft before they are sewn to it from the
ascending aortic graft on the acutely dissected proxi- inside[196].
mal aorta is accomplished by use of teflon felt, tissue Another valve remodelling procedure is less radical:
adhesive such as gelatin resorcinol formaldehyde glue only the Valsalva sinuses are replaced, and the ventricu-
(GRF-glue) or both[198,199]. Regardless of which lar outflow diameter is left at its given size[197]. The
method is applied, the dissected portion of the aorta is aortic sinuses are removed leaving a 3 mm rim along
first completely divided at the level of the sinotubular either side of the line of insertion of the cusp intact. The
junction. Traditionally, the layers of the aorta are then cardiac end of an ascending aortic graft is then scalloped
conjoined by sandwiching them between strips of teflon in such a manner as to accept the triangles of the excised
felt placed inside and outside the dissected perimeter of valve attachments. Next, the strips of aortic wall from
the vessel. This technique is now gradually replaced by where the cusps arise are sutured to the edges of these
glue reconstruction of the dissected layers, a technique triangles before the previously excised coronary buttons
which has turned out to be technically easier and time are connected to appropriate windows in the graft[197].
saving[198]. Application of GRF glue not only produces Whenever the valve may not be preserved and the aortic
a firm union of the dissected layers but also converts root is ectatic, composite grafting as described above
them to a leather like texture. This facilitates secure has remained the standard method for total root
reconstitution of the aortic root greatly, while it replacement in chronic aortic type A dissection.
obliterates any dead spaces below the anastomosis
between graft and aorta at the same time. With either
technique employed, detachment of valve commissures The aortic arch in acute type A (type I and II)
may require resuspension by the use of pledgetted dissection
transmural mattress sutures in addition to reconstruc- Treatment of the acutely dissected aortic arch remains a
tion of the dissected wall layers. much debated subject. The discussion is centred around
the question of when and to what extent the arch should
be replaced. At present there is broad consensus that any
The proximal aorta in chronic type A (type I and II) dissected arch should be explored during a short period
aortic dissection of hypothermic circulatory arrest. In the absence of an
As in acute dissection, the choice for the type of proxi- arch tear an open distal anastomosis of the graft and the
mal repair in chronic dissection depends on the consti- conjoined aortic wall layers at the junction of the
tution of both the aortic root and the valve. In cases ascending and arch portions is made[201,202]. Arch tears
where the root is of normal configuration and the valve occur in up to 30% of patients with acute dissec-
is intact, a supracommisural graft may be implanted. tion[203,204]. If an entry tear traverses the aortic arch, the
Once the commissures are found to be detached, re- distal graft to aortic anastomosis is usually made in such
suspension of one or more leaflets is necessary. This a manner as to replace the arch beyond the entry bearing
represents an adequate valve repair in about 50% of portion. Whenever extensive tears are found, which
patients with chronic type A dissection[199]. In every continue beyond the junction of the transverse and
other case the valve should be replaced before the descending aortic segments, or when there is acute
vascular graft is implanted. dissection of a previously aneurysmatic arch, subtotal or
If the entire root is aneurysmatic, a more radical total arch replacement may be required. This may have
approach is advisable to prevent late dilatation and to include reconnection of some or all supraaortic
recurrent dissection of the remaining aorta. In such vessels to the graft during hypothermic circulatory
instances a composite graft should be implanted since it arrest. The techniques for reconstituting and fortifying
eliminates the entire diseased proximal aortic portion. the dissected layers of the aortic arch are similar to the
As an alternative, xenografts, allografts or autografts ones described for the aortic root; either GRF adhesive
may be implanted in selected cases. The valve sparing or strips of teflon felt are used.

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1667

The aortic arch in chronic type A (type I and II) aortic may warrant timely interventional therapy by catheter
dissection guided fenestration of the dissection membrane thereby
The procedure on the aortic arch is often less demanding decompressing the true lumen of the abdominal aortic
in chronic dissection than in acute dissection because the segment. In case this procedure does not lead to prompt
extent of the aneurysmal dilatation generally dictates the relief of symptoms, surgical intervention is required. All
extent of aortic replacement. Beyond that collagen in- other, uncomplicated type B (type III) aortic dissections
growth will improve the wall quality of the false lumen are usually treated conservatively, since till today there is
over time, making it possible to suture it to the graft if no proven superiority of one particular treatment above
required. As in acute arch dissection, the graft is better another, be it surgical, interventional by stent grafting or
connected to the true channel of the aorta either at the medical.
distal end of its wall delamination or beyond any entry Operative intervention for chronic type B (type III)
tears present in the arch, and thereby reconstituting the aortic dissection is primarily directed to alleviate the
wall layers at this level. If this is not feasible under expansion process and to the threatening or manifest
certain conditions, the anastomosis is made to the firm rupture of the dissected segment. Indications for opera-
wall of the false channel. Late aneurysm formation is tive intervention for post-dissection aneurysms are
always a possibility in such cases. However, in replace- similar to those of other thoracoabdominal aneurysms.
ment procedures extending to the proximal descending The surgical management of both acute and chronic
aorta, the graft is usually anastomosed to the outer dissections of the descending aorta comprises the re-
aortic wall because redirecting distal blood flow to the placement of affected portions with a tubular graft of
true aortic channel does not serve any purpose in view of appropriate length and size. The standard approach to
the presence of multiple downstream reentries. In arch the dissected descending aorta is the conventional fifth
aneurysms extending to the downstream aorta an rib posterolateral chest incision which allows access to
elephant trunk extension of the arch graft is inserted as replace the descending aorta down to the level of the
first described by Borst et al.[205,206]. Total aortic arch eighth intercostal space. According to the extension of
replacement using this technique includes the division of the vessel disease, this incision gives appropriate expo-
the dissected circumference of the distal aorta and the sure of the aorta either through a single or double
removal of the downstream dissecting membrane. This thoracotomy. Most surgeons perform the operation
technique greatly facilitates later procedures on the using extracorporal circulation by means of a left heart
downstream aorta. Instead of performing a conven- bypass. In cases where the replacement has to be
tional anastomosis between the end of the graft and the extended toward the thoracoabdominal segment,
descending aorta, the graft is allowed to float freely in femorofemoral bypass may be preferred.
the aortic lumen. During the subsequent procedure the Usually moderate hypothermia is induced with care
elephant trunk section of the graft may either be con- being taken to equalize perfusion pressures during the
nected to the distal descending portion directly or it is implantation of the graft proximal and distal to the
extended with another tubular prosthesis, which may aortic crossclamp.
then be anastomosed at any desired downstream level of
the aorta.

Summary Surgery in acute type B (type III) dissection.

The indication for surgery in type B (type III) aortic
Surgery in acute type A (type I and II) dissection. dissection is limited to the following criteria
The aim of surgery is to prevent aortic rupture, + persistent, recurrent chest pain
pericardial tamponade, and to relieve aortic regur- + aortic expansion
gitation. Implantation of a composite graft in the + periaortic haematoma
ascending aorta with or without reimplantation of + mediastinal haematoma
coronary arteries is performed. A large variability
of surgical procedures exist.
Management in infancy and childhood
The same principles used for adults apply to the man-
Surgery in type B (type III) aortic dissection agement of dissection and aneurysm in infancy and
There is still a broad consensus that the indications for childhood. There are no measures specific for this age
operative treatment in patients with acute type B (type group. It is thought that dissection will inevitably occur
III) are limited to the prevention or relief of life threat- whenever a part of the arterial tree reaches critical
ening complications such as intractable pain, a rapidly dimensions, just as it holds true for those who have
expanding aortic diameter, periaortic or mediastinal reached skeletal maturity. The major area of controversy
haematoma as signs of aortic rupture. Dissection occur- remains when to intervene prophylactically in order to
ring in a previously aneurysmatic aorta may also be prevent dissection when there is underlying dilatation. Is
considered a surgical emergency. The onset of other the absolute dimension of the aneurysmal segment the
complications such as ischaemia of limbs, kidneys or gut most useful measure, or should a size ratio be used as

Eur Heart J, Vol. 22, issue 18, September 2001

1668 Task Force Report

Table 17 Interventional therapy in aortic dissection

Recommendation Class I IIa IIb III Level of evidence

1. Stenting of obstructed branch origin for static obstruction of branch artery + C

2. Balloon fenestration of dissecting membrane plus stenting of aortic true lumen + C
for dynamic obstruction
3. Stenting to keep fenestration open + C
4. Fenestration to provide re-entry tear for dead-end false lumen + C
5. Stenting of true lumen
+ to seal entry (covered stent) + C
+ enlarge compressed true lumen + C

has been proposed for the root[41,207,208]. What are proposed[212,213]. The first successful endovascular balloon
appropriate upper limits to be used in a growing child to fenestration of a dissecting descending aortic membrane
define these parameters? These factors have yet to be to treat mesenteric ischaemia was described in 1990[216].
agreed. Various reports have been published since[217–224].
Aortic stent grafts were first used to exclude abdomi-
nal and later thoracic true and false aneurysms[225–228].
Interventional therapy by percutaneous The treatment of aortic dissection evolved slowly, how-
ever, because the risk of paraplegia was feared. This
stenting and/or percutaneous fenestration
complication occurs in up to 18% after surgery[229–231].
Introduction However, with further technical improvement a large
Conventional treatment of type A (type I, II) dissection series of aortic dissection cases has now been success-
consists of surgical reconstruction of the ascending aorta fully treated by stent grafts which cover the entry tear in
with restoration of flow, preferentially into the true the descending aorta and even in the aortic arch[232].
lumen. In type B (type III) dissection with ischaemic Moreover the authors demonstrated that the closure of
complications, treatment includes reconstruction of the the entry tear is essential to reduce aortic size. Entry
thoracic aortic segment containing the entry tear[209], tear closure promotes both thrombus formation and
bypass of the compromised organ or limb[210] or surgical healing[232]. Combined surgical and interventional
fenestration[211–213]. Four major patterns of ischaemic procedures have been proposed already[233].
complications can be distinguished, depending on the
characteristics and course of the true and false lumen as
well the major aortic branches involved: Indications for stent placement and
+ Compression of the true lumen in the region of the fenestration
main abdominal branches.
+ Compression of the true aortic lumen proximal to the The exact role of percutaneous fenestration and stent
main abdominal branches. placement in the treatment of aortic dissection has yet to
+ Involvement of aortic main branches in the dis- be determined (Table 17). However, there appears to be
section. a clear-cut indication for fenestration and stent place-
+ Enlarging false aneurysm due to patent proximal ment in the treatment of static or dynamic obstruction
entry tear. of aortic branch arteries.
+ Treatment includes reconstruction of the thoracic + Vessels compromised by static obstruction of a
aortic segment containing the entry tear[209], bypass branch artery are treated by placing endovascular
of the compromised organ or limb[210] or surgical stents across the vessel origin.
fenestration[211–213]. + Vessels compromised by dynamic obstruction are
Approximately 90% of peripheral pulse deficits associated treated by percutaneous balloon fenestration with or
with aortic dissection can be reversed by repairing the without stents in the aortic true lumen.
thoracic aorta[214]. However, patients with mesenteric or In classic aortic dissections, successful fenestration
renal ischaemia do not fare that well. Mortality of patients raises true luminal pressure but leaves false luminal
with renal ischaemia is 50 to 70%[210,212] and mortality pressure unchanged. Sometimes stents have to be de-
figures in mesenteric ischaemia can be as high as 87%[210]. ployed in the true lumen in order to buttress the flap in
The surgical mortality rates in patients with peripheral a stable position remote from branch artery origins[223].
vascular ischaemic complications, however, also amounts In chronic dissection where fenestration of a fibrosed
to up to 87% of those with mesenteric ischae- dissecting membrane may result in collapse of the con-
mia[209,210,213,215], with an 89% hospital mortality nection between true and false lumen, a stent may be
rate[212,213]. The operative mortality of surgical fenestra- necessary to keep the fenestration open[234]. A second
tion is only 21% to 67%, and percutaneous management indication for fenestration is to provide a reentry tear for
of obstructed branch arteries has therefore recently been the dead-end false lumen back into the true lumen. The

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1669

aim of this is to prevent thrombosis of the false lumen high grade compression of the supplying true lumen
which might compromise branches which derive their cranial to major aortic branches, the compressed lumen
supply exclusively from the false or jointly from the false may be enlarged by a stent to increase distal flow.
and true lumen. There are autopsy studies that noted The so called ‘Harrington road’ approach implies the
improved survival in acute classical dissection in patients placement of telescoping stents into the true lumen from
with reentry tears versus those without[235]. On the other the entry tear near the left subclavian artery all the way
hand, this treatment may increase the risk of aortic down past the visceral arteries, and across the bifurca-
rupture in the long-term because a large reentry tear tion, if necessary. This approach is expensive, however,
promotes flow in the false lumen, a fact which provides and if multiple branch origins are covered by stents, the
the basis for aneurysmal degeneration of the false lu- patient is exposed to a long-term risk of branch artery
men[211,223]. There is also a certain risk of peripheral stenosis or distal embolization. Multiple aortic stents
embolism from a patent but partly thrombosed false separated by a certain distance are used unless there is
lumen[211,223,234]. a large pressure gradient between the true and false
The most effective and optimal method to exclude lumen[223]. Sometimes stents have to be placed across the
the aneurysmally dilated false lumen would be the origin of the celiac, superior mesenteric and renal ar-
exclusion of the proximal entry tear with an accept- teries to keep the supplying true lumen patent[236].
able stent graft. In such cases the absence of a distal Long-term follow-up following these complex interven-
reentry tear is desirable[236], and local treatment by tions is not yet available.
fenestration and stents serves only to establish flow to A more sensible method seems to be the creation of a
compromised aortic branches which originate from the large reentry tear where it is needed, followed by stent
false lumen. placement between the tear and the compromised
Compression of the true aortic lumen cranial to the branch. In order not to compromise flow to the distal
main abdominal branches with secondary distal ischae- branches, stent placement across the superior mesenteric
mic changes because a narrowed true lumen is another and renal arteries should be avoided[223]. Balloon ex-
indication for stent placement. The stent will enlarge the pandable Palmaz stents are recommended for precise
compressed true lumen and improve blood flow[224,234]. deployment just cephaled to a critical branch artery
Fenestration and pressure reduction within the false (superior mesenteric artery or renal artery)[223]; 14 mm
lumen still seems to be the optimal choice, however[218]. diameter Wallstents[223,234,236] are an alternative.
Based on the measurements obtained during angiog-
raphy, IVUS, TEE, CT or MRI, the individual graft
Interventional techniques stents are produced with a diameter of 2–4 cm covering
3–5 cm proximal and distal to the tear. Average stent
Technique of percutaneous balloon fenestration grafts are 3·5 cm (2·4–4·5 cm) in diameter and 10·5 cm
The technical goal in percutaneous balloon fenestration (4·5–22·5 cm) long. The right femoral artery is the
is to create a tear in the dissection flap that separates the common site for surgical insertion of the 22–27F
true from the false lumen. It is preferable to perform systems, leaving the left side for percutaneous access to
fenestration from the smaller (usually the true lumen) the aorta for angiography and IVUS. A stiff wire is
into the larger or false lumen. Most commonly a placed after a pigtail catheter has been introduced over a
Roesch-Uchida needle, Brockenborough needle or soft wire.
Colopinto needle is used to perform fenestra- The procedure is performed with the patient under
tion[219,224,234,236]. The fenestration site is chosen close to general anaesthesia. Blood pressure is lowered to 50–
the arteries to be salvaged. After the needle is advanced 60 mmHg by sodium nitroprusside during stent expan-
from the true into the false lumen at the desired sion. Upon stent expansion the aortic pressure would
level — this is very much facilitated by IVUS increase instantaneously because antegrade flow is
monitoring — and following safe placement of a super blocked and will become free after complete stent graft
stiff guidewire into the false lumen, angiography is delivery. After deployment of a stent, a balloon, incor-
performed in both lumina. A balloon catheter of 12 to porated in the system, allows further apposition of the
15 mm diameter and 20–40 mm length is used to create a stent struts to the wall of the true lumen. It is not the aim
transverse tear. If IVUS is not available, a balloon to perform wall wrapping of the intimal flap to the wall
catheter or a Dormia basket placed in the false lumen of the false lumen, but to occlude intimal tears.
can be used as a targeting object for piercing the
dissecting membrane with the needle[220]. It may be Branch vessel stenting
necessary to implant large stents in the range of 10– A dissection that propagates into a branch artery and
14 mm diameter in order to keep the aorta or side causes static obstruction is treated by direct branch
branches open, particularly when the false lumen vessel stents. A stent is indicated when a significant
has already been thrombosed. gradient between the branch artery and the supplying
aortic lumen exists. It is important that the aortic true
Technique of aortic stenting luminal cross section and true lumen pressures are
Aortic stents are primarily used to supplement fenestra- reassessed after flow restoration in large arteries,
tion as well as to reduce the dissection flap. In case of as stenting of arterial branch stenoses can result in

Eur Heart J, Vol. 22, issue 18, September 2001

1670 Task Force Report

significant reorientation of the dissection flap with the Complications of interventional therapy
changed pressures in the supplying aortic lumen. Precise
stent placement is crucial for these branch vessel ob- In view of the fact that the post-procedural mortality
structions. Stents with no or only minimal shortening rate seems largely dependent on the severity and
(or balloon expandable stents, respectively) seem advan- duration of ischaemia before the interventional
tageous for branch vessel stenting. Consequently the procedures — half of the 30 day mortalities (13%) were
Palmaz balloon expandable stent was used in all three due to irreversible damage sustained before the endo-
major series published[224,234,236]. vascular treatment — timely percutaneous treatment
seems mandatory[223]. It is therefore advocated that
patients with acute type A dissection and malperfusion
Results of interventional therapy of peripheral branches should undergo percutaneous
revascularization first, and surgical repair should be
In 57 patients, flow could be restored in more than 90% delayed until the ischaemic injury resolves[239].
(range 92 to 100%) of vessels obstructed from aortic
dissection[223,224,234,235]. The average 30 day mortality
rate was 10% (range 0 to 25%). No additional surgical Summary
revascularization was needed in any of the patients Interventional therapy in aortic dissection provides
treated. Most of the patients remained asymptomatic new approaches to handle complications.
over a mean follow-up time of about one year. All Aortic fenestration with or without stent place-
mortalities were unrelated to the percutaneous pro- ment allows immediate relief of organ malperfusion
cedure and were usually the result of non-reversible for
ischaemic changes, progression of the dissection or + visceral
complications of additional reconstructive surgical pro- + renal
cedures on the thoracic aorta. Two patients died after 3 + limb ischaemia either before or after surgical
and 17 months, respectively, from rupture of the chroni- treatment
cally enlarging false lumen[223]. Potential problems arise Graft stent implantation is an evolving technique
from unpredictable haemodynamic alterations in the which opens new avenues to treat type B (type III)
true and false lumen after fenestration and stenting. dissection. Occlusion of entry tears induces throm-
These alterations may result in loss of previously well bus formation and vessel wall healing.
perfused arteries, as well as in loss of the desired salvage
of compromised arteries. Affected arteries can also be
managed by endovascular techniques such as additional
stent procedures[223,224,234,236]. Follow-up in aortic dissection
First preliminary results of aortic graft stent im-
plantation are currently becoming available[227,228]. It Natural history of aortic dissection and
is already evident that percutaneous application is prognosis
safer and produces better results than surgical graft
stent implantation[228]. Paraplegia seems to occur, Aortic dissection has a prevalence of 0·5 to 2·95/100 000/
too, related to extensive graft stenting but not with yr[240–242] with the highest rate in Italy (4·04/100 000/
short (<15 cm) stents and in consecutive instead of yr)[235]. Mortality is between 3·25–3·6/100 000/yr[244].
single approaches if longer segments have to be Due to the high mortality of aortic dissection in the
stented. Results on short-term follow-up were good, acute stage, the survival rate in both type A and B (type
the tears became well occluded and aortic diameters I–III) dissection is very low. Forty years ago, the 24 h
decreased after complete thrombosis of the false mortality was 21%. After 30 days 8% of patients re-
lumen. This proves that stent placement may facilitate mained alive and only 2% after 1 year[97]. Ten years later
healing of the dissection. Whether or not additional the 48 h mortality was still reported to be 50% or
tears in the abdominal part of the aorta have to be 1%/h[240]. Up to 20% of the patients died before reaching
occluded when entry tears in the thoracic aorta are the hospital. Even recently a mortality of 68% within
closed has to be demonstrated in the future. Endo- 48 h and 1·4%/h was reported in a survey spanning 27
vascular leakages were found, occasionally with years[245]. In this population-based longitudinal study
spontaneous occlusion of some portion of the leak with an incidence of 2·95/100 000/yr the important ob-
and reopening of another during follow-up. In some servation was that the diagnosis was established in only
patients follow-up showed that tears had initially 15% before autopsy. The most important causes of
been overlooked, and additional stents were death were aortic rupture in 80% of the patients[245].
implanted. A dramatic improvement can be observed, due to
Patients can developed an inflammatory reaction medical and surgical therapy over the last 30 years. The
after implantation. This may present as an elevated European Cooperative study group reported a 1 year
C-reactive protein in combination with fever. Both survival rate of 52%, 69% and 70% in type A (type I,
signs may disappear spontaneously as the healing type II) and type B (type III) dissection, respectively.
progresses[236,237]. This decreased to 48%, 50% and 60% after 2 years[6].

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1671

Table 18 Prevention of aortic dissection in inherited diseases (Marfan’s Syndrome, Ehlers-Danlos Syndrome,
annuloaortic ectasia)

Recommendation Class I IIa IIb Level of evidence

1. Life-long beta-adrenergic blockade + C

2. Periodic routine imaging of the aorta + C
3. Prophylactic replacement of the aortic root before diameter exceeds 5·0 cm in + C
patients with family history of dissection
4. Prophylactic replacement of the aortic root before diameter exceeds 5·5 cm + C
5. Moderate restriction of physical activity + C

Similar results were reported by others, also showing a dissection class 1 is found in 15–41%[92,94,256–263], rupture
better prognosis for type B dissection. The 1 year in 5–26%[12,259,263]. Complete healing on the other
survival was 34% and 85%, respectively[246,247]. The hand is found in 11–75% with resolution of the wall
survival seems to be dependent on the degree of com- thickening[94,257,259,261,263,264].
munication, that means the wall stress in the false lumen. During follow-up, ulcerated plaques (class 4) seem to
The best prognosis was found in non-communicating be more malignant with class 1 dissection of the de-
and retrograde type B (type III) dissection limited to the scending aorta: there are more aortic ruptures. Others
descending aorta (80 and 86%, 2 year survival rate reported a more benign course and did not consider
respectively)[6]. immediate surgery[106,108]. However, subintimal hae-
Further improvement has not been reported during matoma and complicated ulcers represent signs of
the last 20 years. The IRAD study reported a mortality emergency with pending rupture. Ulcerated plaques can
of 27% and 29% for type A and B (type I–III) dissection form large pseudoaneurysms[265–267]. Development of
in 464 patients after surgical therapy and 53% and 9% class 1 dissection is found in 10–20%. Traumatic aortic
after medical therapy, respectively[248]. dissection (class 5) has also a poor prognosis, but limited
Spontaneous healing of aortic dissection can occur data are available[268–272].
during medical therapy, but it is rare. The false lumen
disappears and circumscript wall thickening devel-
ops[6,94,111,112,249]. In the European Cooperative study Follow-up in Marfan patients
wall thickening was observed as a sign of healing in only
4% of patients, mainly in type A (type II) and type B The accepted critical aortic root dimension of 5·0–
(type III) dissection[6]. In MRI studies this was observed 5·5 cm may be seen at any age, even in infancy, and
in 7%[250], by CT in 31% of type B (type III) dissec- suggests that intervention is advisable in anticipation of
tions[251]. Continuous flow through large entry tears subsequent dissection, as for the fully grown population
seems to prevent spontaneous healing[6]. (Table 18). The general agreement is, that prophylactic
Another form of healing process is complete throm- replacement of the aortic root should be performed at a
bosis of the false lumen which is sometimes observed diameter of 5·5 cm in Marfan patients[273–278]. A smaller
and appears to be a prerequisite for complete heal- threshold may apply in the very young but the difficulty
ing[6,94,252]. The extent of thrombus formation is also in defining an absolute upper dimension in childhood is
important. This may be related to the fact that patients that growth must be accounted for. The particular
are already in a more chronic stage and the lack of growth upper dimension in childhood is that growth
communication and an increased wall thickness decrease must be taken into account. The particular growth
wall stress. In 2% of patients a type B (type III) pattern of the Marfan phenotype needs to be considered
dissection with communication can continue to dissect as well. Aortic root dimensions (Fig. 2) should be
into the ascending aorta in a retrograde fashion[94]. If the plotted serially (not against age, but against body sur-
aortic arch is involved, the mortality is higher than with face area) at least annually, possibly more frequently in
a type B (type III) dissection limited to the descending very young children, and certainly during the rapid
aorta[6]. adolescent growth spurt. The dimensions assessed by
Present surgical techniques do not result in progres- echocardiography may well lie outside the upper confi-
sion of thrombus formation in patients with aortic dence interval (Fig. 3) for the normal population, but
dissection: replacement of the ascending aorta alone may follow a centile above but parallel to it. Should the
cannot eliminate flow in the false lumen and thrombus dimensions deviate (upward) from the pursued centile,
formation is therefore not likely. Less than 10% of then it is the time to consider intervention[279,280].
operated patients with type I dissection show an It is imperative that further longitudinal studies are
obliteration of the false lumen[6,250–255]. undertaken to define the normal aortic root growth
Currently information about the natural history of pattern in Marfan’s syndrome from very early child-
intramural haematoma (class 2) is limited. The mortality hood. Guidelines for clinical decision should be derived
is high: 20–80%[12,94,101,256]. The development of aortic from such data to decide the minimal deviation from the

Eur Heart J, Vol. 22, issue 18, September 2001

1672 Task Force Report

Table 19 Reoperation following repair of aortic dissection

Recommendation Class I IIa IIb Level of evidence

1. Surgical intervention for

+ secondary aneurysm in dissected aorta remote from initial repair + C
+ recurrent dissection or aneurysm formation at previous intervention site + C
2. Graft replacement for gross dehiscence or infection + C
3. Use of homografts to replace infected protheses + C
4. Endovascular stenting if surgical indication and suitable anatomy + C

norm, with respect to the risk of dissection; but can be to make measurements at identical levels of the aorta. In
accepted. patients after surgical repair of the dissection, knowl-
Consideration should also be given to include replace- edge of the surgical technique performed is essential for
ment of an ectatic aortic root (Table 16), even if it has correct interpretation of all imaging techniques includ-
not reached the accepted dimension for replacement, if ing MRI. The second choice represents TEE, but care-
another cardiac operative procedure is to be undertaken. ful documentation of the scan fields is necessary when
There are no guidelines governing intervention in the question concerning aortic expansion has to be
cases of aneurysmal dilatation of other segments of the answered. CT can also be used and it is the technique
aorta as a prophylactic measure against dissection. It which is most frequently performed. In the age after 60
might be prudent to take action if a sudden or rapid years the negative effect of ionizing X-ray exposure can
expansion is recognized[279,280]. be neglected compared to the severity of the disease.
There is little evidence that exercise in childhood, or Regular assessment of the aorta should be performed
any particular type of activity influences the rate of 1, 3, 6 and 12 months after the acute event, followed by
progression of aortic root dilatation, though there is a yearly examinations. Most important are the aortic
report of a teenager in whom dissection was precipitated diameter, signs of aneurysm formation; haemorrhages at
by (recreational) weight lifting[281]. Advice (Table 19) surgical anastomoses or graft stent sites have to be
concerning exercise is considered important. Blood detected.
pressure should not exceed 130 mmHg systolic; this
holds true for children and adults[281].

Close follow-up for aortic dissection by a special-

Imaging for follow-up studies ized team includes the assessment of
+ signs of aortic expansion
Patients with aortic dissection need close follow-up. The + aneurysm formation
main task is to control blood pressure in order to reduce + signs of leakages at anastomoses/stent sites
wall stress. A level below 135/80 mmHg is advised. This + malperfusion
is the same level as for patients without aortic dissection The single most important factor is excellent blood
but arterial hypertension. Beta-blocking agents are pre- pressure control <135/80 mmHg. After hospital dis-
ferred. Combination therapy with other drugs is usually charge regular outpatient visits at 1, 3, 6 and 12
needed to control the pressure. The recommendation month and thereafter every year are recommended.
concerning blood pressure control should be followed. First choice is MRI, 2nd choice CT and 3nd TEE.
Specialized physicians with a deep insight into the
patients’ history and knowledge of aortic dissection
including different treatment options should follow the
patients in order to detect signs of progression of the Reoperation
disease or aneurysm formation.
To follow patients after medically or surgically treated The majority of late deaths following primary surgery of
acute aortic dissection, MRI appears to be the technique acute aortic dissection has been due to rupture of the
of choice (Table 13). MRI avoids exposure to ionizing aorta[88]. Therefore, timely reoperation (Table 19) is
radiation or nephrotoxic contrast agents used for CT required whenever necessary. There are two principal
and is less invasive than transoesophageal echocardiog- reasons for reoperation. First, the dissected aorta may
raphy. An important consideration in serial studies is the become aneurysmatic (5 to 6 cm in diameter) remote
ease with which serial findings can be compared[282,283]. from the initial repair (Table 20). The second reason
Documentation of MR-studies on a series of prints derives from instances where the dissection had been
rather than video tape facilitates the diagnosis of pro- improperly repaired. The rate of reoperation for type I
gressive enlargement of the false lumen or the entire and type II dissection is about 10% at 5 years and up to
aorta. Moreover, the large field of view permits visual- 40% at 10 years after primary surgery[6,246]. This risk is
ization of neighbouring anatomical landmarks in order even higher in patients with Marfan’s syndrome[277,278].

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1673

Table 20 Therapy of chronic aortic dissection

Recommendation Class I IIa IIb Level of evidence

Type A (type I, II):

1. Indications for surgery as in non-dissecting aneurysm if symptoms or aortic + C
regurgitation or aortic diameter >(5–) 6 cm

Type B (type III):

1. Indications for surgery as in non-dissecting aneurysms if symptoms or progressive + C
aortic enlargement to d6·0 cm
2. Endovascular stenting if surgical indication and suitable anatomy + C

The proximal aorta, particularly the aortic root and tend to collapse which makes dissection of retrosternal
ascending portion is the most common site requiring adhesions and completion of re-sternotomy much easier
reoperation. The underlying causes are generally iatro- and safer. Cardiopulmonary bypass is reinstituted once
genic: the dissection may either have persisted after the the ascending aorta is dissected free and clamped. Then,
primary procedure or may have recurred later. The the core temperature may either be lowered to 20 C
incidence of new dissection including the ascending before re-induction of circulatory arrest whenever the
aorta varies from 0·03 to 0·1%[284–286]. After aortic valve correction of aortic arch pathology is necessary or
replacement, it occurs in 0·5%–1%[76,287–288]. Some con- hypothermia may be maintained during the repair of the
ditions that predispose to subsequent dissection include ascending aorta.
previous aortic valve replacement, congenitally de- The choice of procedure depends on the state of the
formed valves or overlooked annuloaortic ectasia[289,290]. root. In the absence of root ectasia, the dissected wall
Others cases include root aneurysms, redissection after layers may simply be conjoined and anastomosed to an
glue repair or composite replacement[291,292]. ascending aortic tube graft. Depending on the coronary
The key to a successful reoperation on the dissected ostia vis-a-vis the valve’s suturing ring they may be
proximal aorta is safe entry into the chest, while all anastomosed directly to the graft or after mobilizing
subsequent manoeuvres tend to follow the principles of ostial buttons.
standard surgery in this region. Great care must be When performing surgery for complications of a
exercised when performing repeat sternotomy because previously implanted composite graft, several alterna-
the aorta is usually unprotected by the pericardium. This tives may be used. Minor leaks (communications with
is particularly true in cases where an ascending aortic the perigraft space) at the ostial anastomoses or at the
tube graft or an aneurysm is closely adherent to the valve’s insertion line can sometimes be closed directly. In
posterior table of the sternum in association with severe gross dehiscence of the aortic or coronary ostial anasto-
aortic valve incompetence. The approach to these com- moses, particularly if associated with infection, the con-
bined lesions may require deviation from the routine duit is replaced, in the latter case an allograft conduit is
longitudinal sternotomy in order to avoid both fatal preferred.
bleeding and left ventricular overdistension. In such Coronary bypass grafts require particular attention
instances, a fifth-rib bilateral or unilateral thoracotomy when performed in conjunction with surgery on the
with transverse sternotomy and prior institution of proximal aorta. If a left internal mammary artery graft
right atrial-femoral or femoro-femoral bypass are had been placed its pedicle is carefully dissected away
recommended[293]. from the distal anastomosis and its bulk is clamped.
A modification of this approach has been reported Right internal mammary artery grafts will often interfere
for ascending aortic reoperations in the presence of with the aortic procedure and may have to be divided
aortic valve incompetence: instead of completing proximally; ultimately they are anastomosed to the
the re-sternotomy at moderate hypothermia a limited, ascending aortic prosthesis.
inferior re-sternotomy is performed first[294]. Then, dis- Late complications following primary operations on
section of the diaphragmatic aspect of both the left and the aortic arch are encountered less frequently than
right ventricle allows the introduction of an apical vent. those following root and the ascending aortic pro-
With the vent in place, core cooling is continued until cedures[267]. Aneurysmal dilatation of the false channel
the onset of ventricular fibrillation. If inadequate per- of the arch can usually be traced to the arch entries not
fusion pressure prevents sufficient lowering of the tem- being resected or to creation of new tears when the distal
perature, the aorta may be occluded by apical insertion graft to aortic anastomosis was constructed during the
and inflation of a balloon catheter in the ascending aorta primary procedure[296,297]. In these instances reoperative
when clamping of the aorta is impossible because of replacement of that structure may be required. The
tissue stiffness tissue or difficult exposure[295]. At a proximal repair is often left intact. The procedure fol-
rectal temperature of 25 C, circulatory arrest is induced. lows the principles of primary arch replacement: a
Under this condition, the heart and the ascending aorta separate graft is used which is ultimately anastomosed to

Eur Heart J, Vol. 22, issue 18, September 2001

1674 Task Force Report

the proximal prosthesis following resection of the true Adam Torbicki, MD, FESC, Department of Chest
aortic channel. Medicine, Institute of Tuberculosis and Lung Disease,
Warszawa, Poland
Luis A. Providencia, MD, FESC, Department of Cardi-
Appendix 1: ESC Task Force on Aortic ology, Coimbra University, Portugal
Raimund Erbel, MD, FESC, FACC, Department of Appendix 3: ACC Board of Trustees
Cardiology, Essen University, Germany
George Beller, MD, FACC, Department of Internal
Fernando Alfonso, MD, FESC, Interventional Cardi-
Medicine, University of Virginia, Charlottesville, U.S.A.
ology Unit, Hospital Universitario San Carlos, Madrid,
Morton F. Arnsdorf, MD, FACC, Department of Medi-
cine, Cardiology, University of Chicago, Chicago,
Catherine Boileau, Hopital Necker — Enfants Malades,
Clinique Maurice Lamy, France
Marian C. Limacher, MD, FACC, Division of Cardio-
Olaf Dirsch, MD, Department of Pathology, University
vascular Medicine, University of Florida, Gainesville,
Essen, Germany
Bernd Eber, MD, FESC, Department of Internal Medi-
Phyllis M. Tahmasebi, Senior Administrative Coordi-
cine, Hospital of Barmherzige Schwestern, Wels, Austria
nator, ACC
Axel Haverich, MD, Division of Thoracic and Cardio-
vascular Surgery, Hannover Medical School, Germany
(representative of European Society of Cardiac Appendix 4: Evidence-based decision
Surgery) in tabular form
Kjell Radegran, MD, Department of Thoracic Surgery,
Karolinska Hospital, Stockholm, Sweden (represen- In comparison to medical therapy, limited data are
tative of European Society of Cardiac Surgery) available for diagnostic techniques which are required
Harry Rakowski, MD, FACC, Toronto, Canada (rep- in evidence-based medicine for categories A and B.
resentative of the American College of Cardiology, Therefore category C had to be chosen and subclassifi-
president American Society of Echocardiography) cation in relation to the degree of consensus accord-
Udo Sechtem, MD, FESC, Department of Cardi- ing to the ACC/AHA Guideline Classification for
ology and Pulmonology, Robert-Bosch-Krankenhaus, Recommendation.
Stuttgart, Germany
Julien Struyven, MD, Department of Radiology, Hopi- Class I Conditions for which there is evidence or
tal Erasme Université Bruxelles, Belgium (representative general agreement that a given procedure or
of Cardiovascular and Interventional Radiological treatment is useful and effective
Society (CIRSE)) Class II Conditions for which there is conflicting
James F. N. Taylor, Great Ormond Street Hospital for evidence or a divergence of opinion about
Children NHS Trust and the Institute of Child Health, the usefulness/efficacy of a procedure or
London, United Kingdom (representative of European treatment
Society of Paediatric Cardiology) Class IIa weight of evidence /opinion is in favour of
Christoph L. Zollikofer, MD, Institute of Radiology, usefulness/efficacy
Kantonspital Winterthur, Schweiz (representative of Class IIb usefulness/efficacy is less well established by
European Association of Radiology) evidence/opinion
Class III Conditions for which there is evidence and/
or general agreement that the procedure/
treatment is not useful/effective and in some
Appendix 2: ESC Board and SCI cases may be harmful
Committee Reviewers
Maarten Simoons, MD, FESC (President), FACC, Tho-
Financial support
raxcenter, University Hospital Rotterdam, Netherlands The Task Force wishes to express its appreciation for
Lars Ryden, MD, FESC (Past President), FACC, the financial support provided by the Board of the
Department of Cardiology, Karolinska Hospital, European Society of Cardiology.
Stockholm, Sweden
Jean Pierre Bassand, MD, FESC (President elect), The authors thank Dr Zeidan for his help in preparing the
FACC, Department of Cardiology, Pole Coeur manuscript, Mrs Celesnik and Mrs Gerstberger for their intense
Poumon, Univ. Hosp., Jean-Minjoz, Besançon, France secretarial work and Dr Splittgerber for reviewing the English
Werner Klein, MD, FESC (Chairman SCI Committee),
FACC, Department of Cardiology, University Graz,
Barbara Mulder, MD, Academic Medical Centre, [1] Sans S, Kesteloot H, Kromhout D on behalf of the Task
Amsterdam, Netherlands Force. Task Force of the European Society of Cardiology on

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1675

cardiovascular mortality and morbidity statistics. Europe. [25] Furthmayr H, Francke U. Ascending aortic aneurysm with
Eur Heart J 1997; 18: 1231–48. or without features of Marfan syndrome and other fibril-
[2] Godwin JD. Conventional CT of the aorta. J Thorac Imag- linpathies: new insights. Semin Thorac Cardiovasc Surg
ing 1990; 5: 18–31. 1997; 9: 191–205.
[3] Erbel R, Engberding R, Daniel W, Roelandt J, Visser CM, [26] Kantonen I, Savunen T, Peltonen L. Linkage analysis in
Rennollet H. Echocardiography in diagnosis of aortic dissec- Finnish families with annulo-aortic ectasia. Davos, 1996.
tion. Lancet 1989; 1: 457–61. [27] Muluk S, Gertler J, Brewster D et al. Presentation and
[4] Posniak HV, Olson MC, Demos TC, Benjoya RA, Marsan patterns of aortic aneurysms in young patients. J Vasc Surg
RE. CT of thoracic aortic aneurysms. Radiographics 1990; 1994; 20: 880–8.
10: 839–55. [28] OMIM (On line Mendelian Inheritance in Man). http://
[5] Nienaber CA, Spielmann RP, von Kodolitsch Y et al.
Diagnosis of thoracic aortic dissection. Magnetic resonance [29] Darling R, Brewster D, Darling R et al. Are familial abdomi-
imaging versus transesophageal echocardiography. Circu- nal aortic aneurysms different? J Vasc Surg 1989; 10: 39–43.
lation 1992; 85: 434–47. [30] Majumder PP, St. Jean PL, Ferrell RE, Webster MW, Steed
[6] Erbel R, Oelert H, Meyer J et al. Influence of medical and DL. On the inheritance of abdominal aortic aneurysm. Am J
surgical therapy on aortic dissection evaluated by trans- Hum Genet 1991; 48: 164–70.
esophageal echocardiography. Circulation 1993; 87: 1604–15. [31] Verloes A, Sakalihasan N, Koulischer L, Limet R. Aneu-
[7] Beighton P, de Paepe A, Danks D, and 17 co-authors. rysms of the abdominal aorta: familial and genetic aspectes
International nosology of heritable disorders of connective in three hundred thirteen pedigrees. J Vasc Surg 1995; 21:
tissue, Berlin 1986. Am J Med Genet 1988; 29: 581–94. 646–55.
[8] De Paepe A, Devereux R, Dietz H, Hennekam R, Pyeritz R. [32] Pope FM, Narcisi P, Nicholls AC, Germaine D, Pals G,
Revised diagnostic criteria for the Marfan syndrome. Am J Richards AJ. COL3A1 mutations cause variable clinical
Med Genet 1996; 62: 417–26. phenotypes including acrogeria and vascular rupture. Br J
[9] Sakai L, Keene D, Engvall E. Fibrillin, a new 350 kD Dermatol 1996; 135: 163–81.
glycoprotein is a compound of extracellular microfibrills. [33] Roman MJ, Devereux RB, Kramer-Fox R, O’Loughlin J.
J Cell Biol 1986; 103: 2499–509. Two-dimensional echocardiographic aortic root dimensions
[10] Collod G, Babron MC, Jondeau G et al. A second locus for in normal children and adults. Am J Cardiol 1989; 64:
Marfan syndrome maps to chromosome 3p24.2-p25. Nat 507–12.
Genet 1994; 8: 264–8. [34] Ruiz ME, Sty JR, Wells RG. Aortic dissection in a 5-year old
[11] Sood S, Eldadah Z, Krause W, McIntosh I, Dietz H. girl with Marfan’s syndrome. Arch Pediatr Adolesc Med
Mutation in fibrillin-1 and the Marfanoid-craniosynostosis 1996; 150: 440–2.
(Shprintzen-Goldberg) syndrome. Nat Genet 1996; 12: 209– [35] Agarwala BN. Group B streptococcal endocarditis in a
11. neonate. Pediatr Cardiol 1988; 9: 51–3.
[12] Milewicz DM, Michael K, Fisher N, Coselli J, Markello T, [36] Sakurai M, Maeda M, Sai N, Miyahara M, Nakayama M,
Biddinger A. Fibrillin-1 (FBN1) mutations in patients with Takemura H. Aortic dissection in an infant caused by
thoracic aortic aneurysms. Circulation 1996; 94: 2708–11. intraaortic balloon pumping. Pediatr Cardiol 1999 (in press).
[13] Glesby M, Pyeritz R. Association of mitral valve prolapse [37] Vitiello R, McCrindle BW, Nykanen D, Freedom RM,
and systemic abnormalities of connective tissue. A pheno- Benson LN. Complications associated with pediatric cardiac
typic continuum. JAMA 1989; 262: 523–8. catheterization. J Am Coll Cardiol 1998; 32: 1433–40.
[14] Ramirez F. Fibrillin mutations in Marfan syndrome and [38] Crawford ES, Coselli JS, Safi HJ. Reoperations for thoracic
related phenotypes. Curr Opin Genet Dev 1996; 6: 309–15. and thoracoabdominal aneurysms. In: Stark J, Pacifico AD,
[15] Boileau C, Jondeau G, Babron MC et al. Autosomal domi- eds. Reoperations in cardiac surgery. Springer Verlag, 1989:
nant Marfan-like connective-tissue disorder with aortic 361–81.
dilatation and skeletal anomalies not linked to the fibrillin [39] Svensson LG, Crawford ES, Coselli JS, Safi HJ, Hess KR.
genes. Am J Hum Genet 1993; 53: 46–54. Impact of cardiovascular operation on survival in the
[16] Milewicz DM, Pyeritz RE, Crawford ES, Byers PH. Marfan Marfan patients. Circulation 1989; 80: 1 233–42.
syndrome: defective synthesis, secretion and extracellular [40] Gillinov AM, Zehr KJ, Redmond JM, Gott VL, Deitz HC,
matrix formation of fibrillin by cultured dermal fibroblasts. Reitz BA, Laschinger JC, Cameron DE. Cardiac operations
J Clin Invest 1992; 89: 79–86. in children with Marfan’s syndrome: indications and results.
[17] Aoyama T, Francke U, Dietz H, Furthmayer H. Quantita- Ann Thorac Surg 1997; 64: 1140–4; discussion 1144–5.
tive differences in biosynthesis and extracellular deposition of [41] Cavanzo F, Taylor HB. Effect of pregnancy on the human
fibrillin in cultured fibroblasts distinguish five groups of aorta and its relationship to dissecting aneurysms. Am J
Marfan syndrome patients and suggest distinct pathogenetic Obstet Gynecol 1969; 105: 567–8.
mechanisms. J Clin Invest 1994; 94: 130–7. [42] Burks JM, Illes RW, Keating EC, Lubbe WJ. Ascending
[18] Beighton P. ‘The Ehlers-Danlos syndrome’. London: aortic aneurysm and dissection in young adults with bicuspid
William Heinemann Medical Books, 1970. aortic valve: implications for echocardiographic surveillance.
[19] Steinmann B, Royce P, Superti-Furga A. The Ehlers-Danlos Clin Cardiol 1998; 21: 439–43.
syndrome. In: Royce PM, Steinmann B, eds. Connective [43] Harker LA, Slichter SJ, Scott CR, Ross R. Homocystinuria.
Tissue and its heritable disorders. New York: Wiley-Liss Vascular injury and arterial thrombosis. N Engl J Med 1974;
Inc., 1993; 351–407. 291: 537–43.
[20] Biddinger A, Rocklin M, Coselli J, Milewicz DM. Familial [44] Millar AJ, Gilbert RD, Brown RA, Immelman EJ,
thoracic aortic dilatations and dissections: a case control Barkinsher DA, Cywes S. Abdominal aortic aneurysms in
study. J Vasc Surg 1997; 25: 506–11. children. J Pediatr Surg 1996; 31: 1624–8.
[21] Dalgleish R. The human collagen mutation database 1998. [45] Drexler M, Erbel R, Müller U, Wittlich N, Mohr-Kahaly S,
Nucleic Acids Res 1998; 26: 253–5. Meyer J. Measurement of intracardiac dimensions and struc-
[22] Collagen database: tures in normal young adult subjects by transesophageal
[23] Ellis PR, Cooley DA, De Bakey ME. Clinical consideration echocardiography. Am J Cardiol 1990; 65: 1491–6.
and surgical treatment of annuloaortic ectasie. J Thorac [46] Brown OR, DeMots H, Kloster FE, Roberts A, Menashe
Cardiovasc Surg 1961; 42: 363–70. VD, Beals RK. Aortic root dilatation and mitral valve
[24] Coady M, Davies R, Roberts M et al. Familial patterns of prolapse in Marfan’s syndrome: an echocardiographic study.
thoracic aortic aneurysms. Arch Surg 1999; 134: 361–7. Circulation 1975; 52: 651–7.

Eur Heart J, Vol. 22, issue 18, September 2001

1676 Task Force Report

[47] Stein HL, Steinberg I. Selective aortography, the definitive [69] Parmley LF, Mattingly TW, Manion WC, Jahuke EJ. Non-
technique for diagnosis of dissecting aneurysm of the aorta. penetrating traumatic injury of the aorta. Circulation 1958;
Am J Roentgenol Radium Ther Nucl Med 1968; 102: 333– 17: 1086–101.
48. [70] Von Oppell UO, Thierfelder CF, Beningfield SJ, Brink JG,
[48] Hayashi K, Meaney TF, Zelch JV, Tarar R. Aortographic Odell JA. Traumatic rupture of the descending thoracic
analysis of aortic dissection. Am J Roentgenol Radium Ther aorta. S Afr Med J 1991; 79: 595–8.
Nucl Med 1974; 122: 769–82. [71] Ammons MA, Moore EE, Moore FA, Hopeman AR. Intra-
[49] Mohr-Kahaly S, Erbel R. Advantages of biplane and multi- aortic balloon pump for combined myocardial contusion and
plane transesophageal echocardiography for the morphology thoracic aortic rupture. J Trauma 1990; 30: 1606–8.
of the aorta. Am J Card Imaging 1995; 9: 115–20. [72] Dorsa FB, Tunick PA, Culliford A, Kronzon I. Pseudo-
[50] Taylor KM. Diseases of the aorta. In: Julian DG, Camm AJ, aneurysm of the thoracic aorta due to cardiopulmonary
Fox KM, Hall RJC, Poole-Wilson PA, eds. Diseases of the resuscitation: diagnosis by transesophageal echocardiogra-
Heart, 1st edn. London: Bailliere Tindall, 1989: 1338–62. phy. Am Heart J 1992; 123: 1398–400.
[51] Roberts WC. Aortic dissection: anatomy, consequences and [73] Fredman C, Serota H, Deligonul U, Barner H, Pearson A,
causes. Am Heart J 1981; 101: 195–214. Kern MJ. Ascending aortic aneurysm masquerading as fever,
[52] Nevitt MP, Ballard DJ, Hallet JW. Prognosis of abdominal altered mental status and mediastinal mass. Am Heart J
aortic aneurysms. A population-based study. N Engl J Med 1990; 119: 408–10.
1989; 321: 1009–14. [74] Patel KL, Gross J. Extracorporal shock wave lithotripsy
[53] McNamara JJ, Pressler V. Natural history of atherosclerotic induced abdominal aortic aneurysm rupture. J Am Geriatr
thoracic aortic aneurysms. Ann Thorac Surg 1978; 26: 468– Soc 1991; 39: 318–9.
73. [75] Moles VP, Chappuis F, Simonet F, Urban P, De La Serna F,
[54] Masuda Y, Takanashi K, Takasu J, Morooka N, Inagaki Y. Pande AK, Meier B. Aortic dissection as complication of
Expansion rate of thoracic aortic aneurysms and influencing percutaneous transluminal coronary angioplasty. Cathet
factors. Chest 1992; 102: 461–6. Cardiovasc Diagn 1992; 26: 8–11.
[55] Sütsch G, Jenni R, von Segesser L, Turina M. Predictability [76] Pieters FAA, Widdershoven JW, Gerardy AC, Geskes G,
Cheriex EC, Wellens HJ. Risk of aortic dissection after aortic
of aortic dissection as a function of aortic diameter. Eur
valve replacement. Am J Cardiol 1993; 72: 1043–7.
Heart J 1991; 12: 1247–56.
[77] Epperlein S, Mohr-Kahaly S, Erbel R, Kearney P, Meyer J.
[56] Gott VL, Pyeritz RE, Magovern GJ, Cameron DE,
Aorta and aortic valve morphologies predisposing to aortic
McKusick VA. Surgical treatment of aneurysms of the
dissection. An in vivo assessment with transesophageal
ascending aorta in the Marfan syndrome. N Engl J Med
echocardiography. Eur Heart J 1994; 15: 1520–7.
1986; 314: 1070–4.
[78] Leu HJ. Classification of vasculitides. A survey. Vasa 1995;
[57] Bruno L, Prandi M, Colombi P, La Vecchia L. Diagnostic 24: 319–24.
and surgical management of patients with aneurysms of the [79] Churg A, Churg J. Systemic vasculitides, 1st edn. New York,
thoracic aorta with various causes. Br Heart J 1986; 55: Tokyo: Igaku-Shoin, 1991.
81–91. [80] Webster B, Rich C, Densen PM, Moore JE, Nicol CS,
[58] Miller DC. Surgical management of aortic dissections: indi- Padget P. Studies on cardiovascular syphilis. Am Heart J
cations, perioperative management, and long-term results. 1953; 46: 117–45.
In: Doroghazi RM, Slater EE, eds. Aortic dissection. New [81] Boussou H, Julian M, Pieraggi MT. Aortic lathyrism and
York: McGraw-Hill, 1983: 193–243. atheroma in the rat by prolonged hyperlipidic diet. Geron-
[59] Louridas G, Reilly K, Perry MO. The role of the aortic tology 1978; 24: 250–65.
aneurysm diameter to aortic diameter ratio in predicting the [82] Boor PJ, Gotlieb AI, Joseph EC, Kerns WD, Roth RA,
risk of rupture. S Afr Med J 1990; 78: 642–3. Tomaszewski KE. Chemical-induced vasculature injury.
[60] Lemon DK, White CW. Annuloaortic ectasia: angiographic, Summary of the symposium presented at the 32nd annual
hemodynamic and clinical comparison with aortic valve meeting of the Society of Toxicology, New Orleans,
insufficiency. Am J Cardiol 1978; 41: 482–6. Lousiana, March 1993. Toxicol Appl Pharmacol 1995; 132:
[61] McDonald GR, Schaff HV, Pyeritz RE, McKusick VA, Gott 177–95.
VL. Surgical management of patients with the Marfan syn- [83] Dewar WA, Wight PA, Pearson RA, Gentle MJ. Toxic
drome and dilatation of the ascending aorta (authors transl). effects of high concentrations of zinc oxide in the diet of the
J Thorac Cardiovasc Surg 1981; 81: 180–6. chick and laying hen. Br Poult Sci 1983; 24: 397–404.
[62] White RD, Lipton MJ, Higgins CB et al. Noninvasive [84] Grannis FW Jr, Bryant C, Caffaratti JD, Turner AF. Acute
evaluation of suspected thoracic aortic disease by contrast- aortic dissection associated with cocaine abuse. Clin Cardiol
enhanced computed tomography. Am J Cardiol 1986; 57: 1988; 11: 572–4.
282–90. [85] Rashid J, Eisenberg MJ, Topol EJ. Cocaine-induced aortic
[63] Tjon-A-Meeuw L, Bollinger A. [Aneurysm of the abdominal dissection. Am Heart J 1996; 132: 1301–4.
aorta. Diagnosis and indications for therapy]. Schweiz Med [86] Crawford ES, Svensson LG, Coselli JS, Safi HJ, Hess KR.
Wochenschr 1991; 121: 683–92. Surgical treatment of aneurysm and/or dissection of the
[64] Stefanadis CI, Karayannacos PE, Boudoulas HK et al. ascending aorta, transverse aortic arch, and ascending aorta
Medial necrosis and acute alterations in aortic distensibility and transverse aortic arch. Factors influencing survival in
following removal of the vasa vasorum of canine ascending 717 patients. J Thorac Cardiovasc Surg 1989; 98: 659–74;
aorta. Cardiovasc Res 1993; 27: 951–6. discussion 673–4.
[65] Mohr-Kahaly S, Erbel R, Stähn P, Hake U, Oelert H, Meyer [87] De Bakey ME, McCollum CH, Crawford ES et al. Dissec-
J. [Quantitative detection of changes in the thoracic aorta in tion and dissecting aneurysms of the aorta: twenty-year
patients with chronic aortic dissection using transesophageal follow-up of five hundred and twenty-seven patients treated
echocardiography]. Z Kardiol 1999; 88: 507–13. surgically. Surgery 1982; 92: 1118–34.
[66] Kunz R. [Aneurysms in 35,380 autopsies]. Schweiz Med [88] Reul GJ, Cooley DA, Hallman GL, Reddy SB, Kyger ER
Wschr 1980; 110: 142–8. 3rd, Wukasch DC. Dissecting aneurysm of the descending
[67] Young R, Ostertag H. [Incidence etiology and risk of rupture aorta. Arch Surg 1975; 110: 632–40.
of aortic aneurysm. An autopsy study]. Dtsch Med Wschr. [89] Svensson LG, Labib SB, Eisenhauer AC, Butterly JR. Inti-
1987; 112: 1253–6. mal tear without hematoma. Circulation 1999; 99: 1331–6.
[68] Reed D, Reed C, Stemmermann G, Hayashi T. Are aortic [90] Yamada T, Tada S, Harada J. Aortic dissection with-
aneurysms caused by atherosclerosis? Circulation 1992; 85: out intimal rupture: diagnosis with MR imaging and CT.
205–11 Radiology 1988; 168: 347–52.

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1677

[91] Mohr-Kahaly S, Erbel R, Kearney P, Puth M, Meyer J. [115] Hagan PG, Nienaber CA, Isselbacher EM et al. The inter-
Aortic intramural hematoma visualized by transesophageal national registry of acute aortic dissection (IRAD): new
echocardiography: findings and prognostic implications. J insights into an old disease. JAMA 2000; 283: 897–903.
Am Coll Cardiol 1994; 23: 658–64. [116] Slater EE. Aortic Dissection: Presentation and diagnosis. In:
[92] Nienaber CA, von Kodolitsch Y, Petersen B et al. Intramural Doroghazi RM, Slater EE, eds. Aortic Dissection. New
hemorrhage of the thoracic aorta. Diagnostic and therapeu- York: McGraw-Hill, 1983: 61–70.
tic implications. Circulation 1995; 92: 1465–72. [117] Fann JI, Sarris GE, Mitchell RS et al. Treatment of patients
[93] Roberts CS, Roberts WC. Aortic dissection with the en- with aortic dissection presenting with peripheral vascular
trance tear in the descending thoracic aorta. Ann Surg 1991; complications. Ann Surg 1990; 212: 705–13.
213: 356–68. [118] Roth JA, Parekh MA. Dissecting aneurysms perforating the
[94] Mohr-Kahaly S, Erbel R, Rennollet H et al. Ambulatory esophagus. N Engl J Med 1978; 299: 776.
follow-up of aortic dissection by transesophageal two- [119] Spitzer S, Blanco G, Adam A, Spyrou PG, Mason D.
dimensional and color-coded Doppler echocardiography. Superior vena cava obstruction and dissecting aortic aneu-
Circulation 1989; 80: 24–33. rysm. JAMA 1975; 233: 164–5.
[95] Krükenberg E. Beiträge zur Frage des Aneurysma dissecans. [120] Buja LM, Ali N, Fletcher RD, Roberts WC. Stenosis of the
Allg Path 1920; 67: 329–51. right pulmonary artery: a complication of acute dissecting
[96] Gore I. Pathogenesis of dissecting aneurysm of aorta. Arch aneurysm of the ascending aorta. Am Heart J 1972; 83:
Path Lab Med 1952; 53: 142–53. 89–92.
[97] Hirst AE Jr, Johns VJ Jr, Kime SW Jr. Dissecting aneurysm [121] Yamada E, Matsumura M, Kyo S, Omoto R. Usefulness of
of the aorta: a review of 505 cases. Medicine 1958; 37: a prototype intravascular ultrasound imaging in evaluation
217–79. of aortic dissection and comparison with angiographic study,
[98] Klotz O, Simpson W. Spontaneous rupture of aorta. Am J transesophageal echocardiography, computed tomography,
Med SC 1932; 184: 455–73. and magnetic resonance imaging. Am J Cardiol 1995; 75:
[99] Stellwag-Carion C, Pollak St. [Idiopathic aortic rupture as a 161–5.
cause of sudden death]. Beitr Gerichtl Med 1978; 36: 307–17. [122] Spittell PC, Spittell JA Jr, Joyce JW et al. Clinical features
[100] Weintraub AR, Erbel R, Gorge G et al. Intravascular and differential diagnosis of aortic dissection: experience with
ultrasound imaging in acute aortic dissection. J Am Coll 236 cases (1980 through 1990). Mayo Clin Proc 1993; 68:
Cardiol 1994; 24: 495–503. 642–51.
[101] Alfonso F, Goicolea J, Aragoncillo P, Hernandez R, Macaya [123] Kamp TJ, Goldschmidt-Clermont PJ, Brinker JA, Resar JR.
C. Diagnosis of aortic intramural hematoma by intravascular
Myocardial infarction, aortic dissection, and thrombolytic
ultrasound imaging. Am J Cardiol 1995; 76: 735–8. therapy. Am Heart J 1994; 128: 1234–7.
[102] Zotz R, Erbel R, Meyer J. Noncommunicating intrawall
[124] Hartnell GG, Wakeley CJ, Tottle A, Papouchado M, Wilde
hematoma as an early sign aortic dissection. J Am Soc
RP. Limitations of chest radiography in discriminating be-
Echocardiogr 1991; 4: 636–8.
tween aortic dissection and myocardial infarction: implica-
[103] O’Gara PT, DeSanctis RW. Acute aortic dissection and its
tions for thrombolysis. J Thorac Imaging 1993; 8: 152–5.
variants. Circulation 1995; 92: 1376–8.
[104] Shimizu H, Yohino H, Udagawa H et al. Prognosis of [125] Suzuki T, Katoh H, Watanabe M et al. Novel biochemical
intramural hemorrhage compared with classic aortic dissec- diagnostic method for aortic dissection. Results of a prospec-
tive study using an immunoassay of smooth muscle myosin
tion. Am J Cardiol 2000; 85: 792–5.
[105] Stanson AV, Kazmier FJ, Hollier LH et al. Penetrating heavy chain. Circulation 1996; 93: 1244–9.
atherosclerotic ulcers of the thoracic aorta: natural history [126] Sarasin FP, Louis-Simonet M, Gaspoz JM, Junod AF.
and clinicopathologic correlations. Ann Vasc Surg 1986; 1: Detecting acute thoracic aortic dissection in the emergency
15–23. department: time constraints and choice of the optimal
[106] Cooke JP, Kazmier FJ, Orszulak TA. The penetrating aortic diagnostic test. Ann Emerg Med 1996; 28: 278–88.
ulcer: pathologic manifestations, diagnosis and management. [127] DeSanctis RW, Doroghazi RM, Austen WG, Buckley MJ.
Mayo Clin Proc 1988; 63: 718–25. Aortic dissection. N Engl J Med 1987; 317: 1060–7.
[107] Yucel EK, Steinberg FL, Egglin TK, Geller SC, Waltman [128] Banning AP, Masani ND, Ikram S, Fraser AG, Hall RJ.
AC, Athanasoulis CA. Penetrating aortic ulcers: diagnosis Transesophageal echocardiography as the sole diagnostic
with MR imaging. Radiology 1990; 177: 779–81. investigation in patients with suspected thoracic aortic dis-
[108] Kazerooni EA, Bree RL, Williams DM. Penetrating athero- section. Br Heart J 1994; 72: 461–5.
sclerotic ulcers of the descending thoracic aorta: evaluation [129] Isselbacher EM, Cigarroa JE, Eagle KA. Cardiac tamponade
with CT and distinction from aortic dissection. Radiology complicating proximal aortic dissection. Is pericardiocentesis
1992; 183: 759–65. harmful? Circulation 1994; 90: 2375–8.
[109] Braverman AC. Penetrating atherosclerotic ulcers of the [130] Eagle KA. Current management of aortic dissection — data
aorta. Curr Opin Cardiol 1994; 9: 591–7. from the International Registry for Aortic Dissection
[110] Movsowitz HD, Lampert C, Jacobs LE, Kotler MN. Pen- (IRAD). Eur Soc Cardiol 1999; 3278.
etrating atherosclerotic aortic ulcers. Am Heart J 1994; 128: [131] Bolognesi R, Manca C, Tsialtas D et al. Aortic intramural
1210–7. hematoma: an increasingly recognized aortic disease. Cardi-
[111] Erbel R, Bednarczyk I, Pop T et al. Detection of dissection of ology 1998; 89: 178–83.
the aortic intima and media after angioplasty of coarctation [132] Moriyama Y, Shiota K, Hisatomi K et al. Acute type A
of the aorta. An angiographic, computer tomographic, and aortic dissection following intramural hematoma of the
echocardiographic comparative study. Circulation 1990; 81: aorta. A case report. Angiology 1997; 48: 839–41.
805–14. [133] Kang DH, Song JK, Song MG et al. Clinical and echo-
[112] Alfonso F, Almeria C, Fernandez-Ortiz A et al. Aortic cardiographic outcomes of aortic intramural haemorrhage
dissection occurring during coronary angioplasty: angio- compared with acute aortic dissection. Am J Cardiol 1998;
graphic and transesophageal echocardiographic findings. 81: 202–6.
Cathet Cardiovasc Diagn 1997; 42: 412–5. [134] Flachskampf FA, Banbury M, Smedira N, Thomas JD,
[113] Slater EE, DeSanctis RW. The clinical recognition of dissect- Garcia M. Transesophageal echocardiography diagnosis of
ing aortic aneurysm. Am J Med 1976; 60: 625–33. intramural hematoma of the ascending aorta: a word of
[114] Svensson LG, Crawford ES. Aortic dissection and aortic caution. J Am Soc Echocardiogr 1999; 12: 866–70.
aneurysm surgery: clinical observations, experimental inves- [135] Baur A, Stabler A, Bittmann I, Marmarakis G, Reiser M.
tigations and statistical analyses. Part II. Curr Probl Surg [Penetrating aortic ulceration: an unusual form of aortic
1992; 29: 913–1057. dissection]. Fortschr Rontgenstr 1998; 168: 550–6.

Eur Heart J, Vol. 22, issue 18, September 2001

1678 Task Force Report

[136] Just M, Mohr-Kahaly S, Kreitner KF et al. [Magnetic [157] Iliceto S, Ettore G, Francisco G, Antonelli G, Biasco G,
resonance tomography of chronic aortic dissection]. Fortschr Rizzon P. Diagnosis of aneurysm of the thoracic aorta.
Rontgenstr 1993; 158: 109–14. Comparison between two non invasive techniques: two-
[137] Sommer T, Fehske W, Holzknecht N et al. Aortic dissection: dimensional echocardiography and computed tomography.
a comparative study of diagnosis with spiral CT, multiplanar Eur Heart J 1984; 5: 545–55.
transesophageal echocardiography, and MR imaging. Radi- [158] Guéret P, Sénéchal C, Roudaut R. Comparison of trans-
ology 1996; 199: 347–52. esophageal and transthoracic echocardiography in acute
[138] Nienaber CA, von Kodolitsch Y. [Diagnostic imaging of aortic dissection. A multicenter prospective study. J Am Coll
aortic diseases]. Radiologe 1997; 37: 402–9. Cardiol 1991; 17: 264.
[139] von Segesser LK, Genoni M, Kunzli A et al. Surgery for [159] Nienaber CA, Spielmann RP, von Kodolitsch Y et al.
ruptured thoracic and thoraco-abdominal aortic aneurysms. Diagnosis of thoracic aortic dissection. Magnetic resonance
Eur J Cardiothorac Surg 1996; 10: 996–1001; discussion imaging versus transesophageal echocardiography. Circu-
1002. lation 1992; 85: 434–47.
[140] Murgo S, Dussaussois L, Golzarian J et al. Penetrating [160] Nienaber CA, von Kodolitsch Y, Nicolas V et al. The
atherosclerotic ulcer of the descending thoracic aorta: treat- diagnosis of thoracic aortic dissection by noninvasive imag-
ment by endovascular stent-graft. Cardiovasc Intervent ing procedures. N Engl J Med 1993; 328: 1–9.
Radiol 1998; 21: 454–8. [161] Kersting-Sommerhoff BA, Higgins CB, White RD,
[141] Eggebrecht H, Baumgart D, Herold U, Jakob H, Erbel R. Sommerhoff CP, Lipton MJ. Aortic dissection: Sensitivity
Multiple penetrating atherosclerotic ulcers of the abdominal and specificity of MR imaging. Radiology 1988; 166: 651–5.
aorta: treatment by endovascular stent-graft placement. [162] Yang PC, Kerr AB, Liu AC et al. New real-time interactive
Heart 2001; 85: 526. cardiac magnetic resonance imaging system complements
[142] Kaji S, Nishigami K, Akasaka T et al. Prediction of progres- echocardiography. J Am Coll Cardiol 1998; 32: 2049–56.
sion or regression of type A aortic intramural haematoma by [163] Prince MR, Narasimham DL, Jacoby WT et al. Three-
computed tomography. Circulation 1999; 100: II-281–6. dimensional gadolinium-enhanced MR angiography of the
[143] Zotz R, Stern H, Mohr-Kahaly S et al. [Coronary insuffi- thoracic aorta. Am J Roentgenol 1996; 166: 1387–97.
ciency in type II aortic dissection]. Z Kardiol 1987; 76: 784–6. [164] Krinsky GA, Rofsky NM, DeCorato DR et al. Thoracic
[144] Kern MJ, Serota H, Callicoat P et al. Use of coronary aorta: comparison of gadolinium-enhanced three-
arteriography in the preoperative management of patients dimensional MR angiography with conventional MR imag-
undergoing urgent repair of the thoracic aorta. Am Heart J ing. Radiology 1997; 202: 183–93.
1990; 119: 143–8.
[165] Deutsch HJ, Sechtem U, Meyer H, Theissen P, Schicha H,
[145] Creswell LL, Kouchoukos NT, Cox JL Rosenbloom M. Erdmann E. Chronic aortic dissection: comparison of MR
Coronary artery disease in patients with type A aortic imaging and transesophageal echocardiography. Radiology
dissection. Ann Thorac Surg 1995; 59: 585–90. 1994; 192: 645–50.
[146] Pereira L, Levran O, Ramirez F et al. A molecular approach
[166] Wagner S, Auffermann W, Buser P et al. Diagnostic accuracy
to the stratification of cardiovascular risk in families with
and estimation of the severity of valvular regurgitation from
Marfan’s syndrome. N Engl J Med 1994; 331: 148–53.
the signal void on cine magnetic resonance images. Am Heart
[147] Lee B, Godfrey M, Vitale E et al. Linkage of Marfan
J 1989; 118: 760–7.
syndrome and a phenotypically related disorder to two
[167] Pelc NJ, Herfkens RJ, Shimakawa A, Enzmann DR. Phase
different fibrillin genes. Nature 1991; 352: 330–4.
[148] Godfrey M, Vandemark N, Wang M et al. Prenatal diagnosis contrast cine magnetic resonance imaging. Magn Reson Q
and a donor splice site mutation in fibrillin in a family with 1991; 7: 229–54.
Marfan syndrome. Am J Hum Genet 1993; 53: 472–80. [168] Honda T, Hamada M, Matsumoto Y, Matsouka H, Hiwada
[149] Rantamaki T, Raghunath M, Karttunen L, Lonnqvist L, K. Diagnosis of Thrombus and Blood Flow in Aortic
Child A, Peltonen L. Prenatal diagnosis of Marfan Aneurysm using Tagging Cine Magnetic Resonance Imag-
syndrome: identification of a fibrillin-1 mutation in chorionic ing. Int J Angiol 1999; 8: 57–61.
villus sample. Prenat Diag 1995; 15: 1176–81. [169] van Rossum AC, Post JC, Visser CA. Coronary imaging
[150] Sermon K, Lissens W, Messiaen L et al. Preimplantation using MRI. Herz 1996; 21: 97–105.
genetic diagnosis of Marfan syndrome with the use of [170] Solomon SL, Brown JJ, Glazer HS, Mirowitz SA, Lee JK.
fluorescent polymerase chain reaction and the Automated Thoracic aortic dissection: pitfalls and artifacts in MR
Laser Fluorescence DNA Sequencer. Fertil Steril 1999; 71: imaging. Radiology 1990; 177: 223–8.
163–6. [171] Wolff KA, Herold CJ, Tempany CM, Parravano JG,
[151] Mintz GS, Kotler MN, Segal BL, Parry WR. Two- Zerhouni EA. Aortic dissection: atypical patterns seen at
dimensional echocardiographic recognition of the descending MR imaging. Radiology 1991; 181: 489–95.
thoracic aorta. Am J Cardiol 1979; 44: 232–8. [172] Robb GP, Steinberg I. Visualization of chambers of heart,
[152] Khandheria BK, Tajik AJ, Taylor CL et al. Aortic dissec- pulmonary circulation and great blood vessels in man: a
tion: review of value and limitations of two-dimensional practical method. Am J Roentgenol 1939; 41: 1–17.
echocardiography in a six-year experience. J Am Soc [173] Dinsmore RE, Rourke JA, DeSanctis RW, Harthorne JW,
Echocardiogr 1989; 2: 17–24. Austen WG. Angiographic findings in dissecting aortic
[153] Keren A, Kim CB, Hu BS, Eyngorina I et al. Accuracy of aneurysm. N Engl J Med 1966; 275: 1152–7.
biplane and multiplane transesophageal echocardiography in [174] Shuford WH, Sybers RG, Weens HS. Problems in the
diagnosis of typical acute aortic dissection and intramural aortographic diagnosis of dissecting aneurysms of the aorta.
hematoma. J Am Coll Cardiol 1996; 28: 627–36. N Engl J Med 1969; 280: 225–31.
[154] Buck TH, Gorge G, Hunold P, Erbel R. Three-dimensional [175] Sanders C. Current role of conventional and digital aortog-
imaging in aortic disease by lighthouse transesophageal raphy in the diagnosis of aortic disease. J Thorac Imaging
echocardiography using intravascular ultrasound catheters. 1990; 5: 48–59.
J Am Soc Echocardiogr 1998; 11: 243–58. [176] Williams DM, Lee DY, Hamilton BH et al. The dissected
[155] Erbel R, Mohr-Kahaly S, Oelert H et al. Diagnostic strat- aorta: part III. Anatomy and radiologic diagnosis of branch
egies in suspected aortic dissection: comparison of computed vessel compromise. Radiology 1997; 203: 37–44.
tomography, aortography and transesophageal echocardiog- [177] Rackson ME, Lossef SV, Sos TA. Renal artery stenosis
raphy. Am J Card Imaging 1990; 4: 157–72. in patients with aortic dissections: increasing prevalence.
[156] Perry GJ, Helmcke F, Nanda NC, Byard C, Soto B. Evalu- Radiology 1990; 177: 555–8.
ation of aortic insufficiency by Doppler color flow mapping. [178] Khandheria BK. Aortic dissection: the last frontier. Circu-
J Am Coll Cardiol 1987; 9: 952–9. lation 1993; 87: 1765–8.

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1679

[179] Cigarroa JE, Isselbacher FM, De Sanctis RW, Eagle KA. [200] Frater RW. Aortic valve insufficiency due to aortic dila-
Diagnostic imaging in the evaluation of suspected aortic tation: correction by sinus rim adjustment. Circulation 1986;
dissection. Old standards and new directions. N Engl J Med 74 I: 136–42.
1993; 328: 35–43. [201] Ergin MA, O’Connor J, Guinto R, Griepp RB. Experience
[180] Chirillo F, Cavallini C, Longhini C et al. Comparative with profound hypothermia and circulatory arrest in the
diagnostic value of transesophageal echocardiography and treatment of aneurysms of the aortic arch. Aortic arch
retrograde aortography in the evaluation of thoracic aortic replacement for acute aortic arch dissections. J Thorac
dissection. Am J Cardiol 1994; 74: 590–5. Cardiovasc Surg 1982; 84: 649–55.
[181] Eagle KA, Quertermous T, Kritzer GA et al. Spectrum of [202] Heinemann M, Laas J, Jurmann M, Karck M, Borst HG.
conditions initially suggesting acute aortic dissection but Surgery extended into the aortic arch in acute type A
with negative aortograms. Am J Cardiol 1986; 57: 322–6. dissection. Indications, techniques and results. Circulation
[182] Bansal RC, Chandrasekaran K, Ayala K, Smith DC. Fre- 1991; 84: III25–30.
quency and explanation of false negative diagnosis of aortic [203] Bachet J, Guilmet D, Goudot B et al. Cold cerebroplegia. J
dissection by aortography and transesophageal echocardiog- Thorac Cardiovasc Surg 1991; 102: 85–93; discussion 93–4.
raphy. J Am Coll Cardiol 1995; 25: 1393–401. [204] Griepp RB, Ergin MA, Lansman SL, Galla JD, Pogo G. The
[183] Deeb GM, Williams DM, Bolling SF et al. Surgical delay for physiology of hypothermic circulatory arrest. Semin Thorac
acute type A dissection with malperfusion. Ann Thorac Surg Cardiovasc Surg 1991; 3: 188–93.
1997; 64: 1669–75; discussion 1675–7. [205] Borst HG, Walterbusch G, Schaps D. Extensive aortic
[184] Gorge G, Ge J, Haude M, Baumgart D, Buck T, Erbel R. replacement using ‘elephant trunk’ prosthesis. Thorac Car-
Initial experience with a steerable intravascular ultrasound diovasc Surg 1983; 31: 37–40.
catheter in the aorta and pulmonary artery. Am J Cardiac [206] Borst HG, Frank G, Schaps D. Treatment of extensive aortic
Imaging 1995; 9: 180–4. aneurysms by a new multiple-stage approach. J Thorac
[185] Bruce CJ, Packer DL, Seward JB. Transvascular Imaging: Cardiovasc Surg 1988; 95: 11–3.
Feasibility Study Using a Vector Phase Array Ultrasound [207] Yoshinaga M, Oku S, Nomura Y, Nagai E. A case of
Catheter. Echocardiography 1999; 16: 425–30. Marfan syndrome in an adolescent with aortic dissection:
[186] Borst HG, Lass J, Haverich A. A new look at acute type-A should the recommendation for surgical intervention be
dissection of the aorta. Eur J Cardiothorac Surg 1987; 1: changed? Pediatr Cardiol 1999; 20: 431–4.
186–9. [208] Treasure T. Elective replacement of the aortic root in
[187] Lemole GM, Strong MD, Spagna PM, Karmilowicz NP. Marfan’s syndrome. Br Heart J 1993; 69: 101–3.
Improved results for dissecting aneurysms. Intraluminal [209] Walker PJ, Miller DC. Aneurysmal and ischaemic compli-
sutureless prosthesis. J Thorac Cardiovasc Surg 1982; 83: cations of type B (type III) aortic dissections. Semin Vasc
249–55. Surg 1992; 5: 198–214.
[188] Najafi H, Dye WS, Javid H, Hunter JA, Goldin MD, Julian [210] Cambria RP, Brewster DC, Gertler J et al. Vascular compli-
OC. Acute aortic regurgitation secondary to aortic dissec- cations associated with spontaneous aortic dissection. J Vasc
tion. Surgical management without valve replacement. Ann Surg 1988; 7: 199–209.
Thorac Surg 1972; 14: 474–82. [211] Elefteriades JA, Hammond GL, Gusberg RJ, Kopf GS,
[189] Culliford AT, Ayvaliotis B, Shemin R, Colvin SB, Isom OW, Baldwin JC. Fenestration revisited: a safe and effective
Spencer FC. Aneurysms of the ascending aorta and trans- procedure for descending aortic dissection. Arch Surg 1990;
verse arch: surgical experience in 80 patients. J Thorac 125: 786–90.
Cardiovasc Surg 1982; 82: 701–10. [212] Laas J, Heinemann M, Schaefers HJ, Daniel W, Borst HG.
Management of thoracoabdominal malperfusion in aortic
[190] Miller DC. Surgical management of acute aortic dissection:
dissection. Circulation 1991; 84: III20–4.
new data. Semin Thorac Cardiovasc Surg 1991; 3: 225–37.
[213] Elefteriades JA, Hartleroad J, Gusberg RJ et al. Long-term
[191] Fraser CD, Wang N, Mee RB et al. Repair of insufficient experience with descending aortic dissection: the
bicuspid aortic valves. Ann Thorac Surg 1994; 58: 386–90.
complication-specific approach. Ann Thorac Surg 1992; 53:
[192] Gott VL, Cameron DE, Pyeritz RE et al. Composite graft 11–20; discussion 20–1.
repair of Marfan aneurysm of the ascending aorta: results in [214] Fann JI, Sarris GE, Sarris GE, Mitchell RS et al. Treatment
150 patients. J Card Surg 1994; 9: 482–9. of patients with aortic dissection presenting with peripheral
[193] Kouchoukos NT, Wareing TH, Murphy SF, Perrillo JB. vascular complications. Ann Surg 1990; 212: 705–13.
Sixteen-year experience with aortic root replacement. Results [215] Miller DC, Mitchell RS, Oyer PE, Stinson EB, Jamieson SW,
in 172 operations. Ann Surg 1991; 214: 308–18: discussion Shumway NE. Independent determinants of operative mor-
318–20. tality for patients with aortic dissections. Circulation 1984;
[194] Bentall H, De Bono A. A technique for complete replace- 70: 153–64.
ment of the ascending aorta. Thorax 1968; 23: 338–9. [216] Williams DM, Brothers TE, Messina LM. Relief of mes-
[195] Kouchoukos NT, Karp RB, Blackstone EH, Kirklin JW, enteric ischaemia in type III aortic dissection with percu-
Pacifico AD, Zorn GL. Replacement of the ascending aorta taneous fenestration of the aortic septum. Radiology 1990;
and aortic valve with a composite graft. Results in 86 174: 450–2.
patients. Ann Surg 1980; 192: 403–13. [217] Cowling MG, Redwood D, Buckenham TM. Case report:
[196] David TE, Feindel CM. An aortic valve-sparing operation critical lower limb ischaemia due to aortic dissection relieved
for patients with aortic incompetence and aneurysm of by percutaneous transfemoral fenestration. Clin Radiol 1995;
the ascending aorta. J Thorac Cardiovasc Surg 1992; 103: 50: 654–7.
617–21; discussion 622. [218] Faykus MH Jr, Hiette P, Koopot R. Percutaneous fenestra-
[197] Sarsam MA, Yacoub M. Remodeling of the aortic valve tion of a type I aortic dissection for relief of lower extremity
annulus. J Thorac Cardiovasc Surg 1993; 105: 435–8. ischaemia. Cardiovasc Intervent Radiol 1992; 15: 183–5.
[198] Bachet J, Gigou F, Laurian C, Bical O, Goudot B, Guilmet [219] Gorge G, Erbel R. [Intravascular ultrasound for monitoring
D. Four-year clinical experience with the gelatin-resorcine- percutaneous fenestration of a membrane from an aortic
formol biological glue in acute aortic dissection. J Thorac dissection]. Dtsch Med Wochenschr 1996; 121: 1598–602.
Cardiovasc 1982; 83: 212–7. [220] Trerotola SO. Use of a stone basket as a target during
[199] Pego-Fernandes PM, Stolf NA, Moreira LF, Pereira Barreto fenestration of aortic dissection. J Vasc Interv Radiol 1996;
AC, Bittencourt D, Jatene AD. Management of aortic insuf- 7: 687–90.
ficiency in chronic aortic dissection. Ann Thorac Surg 1991; [221] Kato N, Sakuma H, Takeda K, Hirano T, Nakagawa T.
51: 438–42. Relief of acute lower limb ischaemia with percutaneous

Eur Heart J, Vol. 22, issue 18, September 2001

1680 Task Force Report

fenestration of intimal flap in a patient with type III aortic [243] Bickerstaff LK, Pairolero PC, Hollier LM et al. Thoracic
dissection — a case report. Angiology 1993; 44: 755–9. aortic aneurysms: a population based study. Surgery 1982;
[222] Saito S, Arai H, Kim K, Aoki N, Tsurugida M. Percu- 92: 1103–8.
taneous fenestration of dissecting intima with a transseptal [244] Fowkes FG, Macintyre CC, Ruckley CV. Increasing inci-
needle. Cathet Cardiovasc Diagn 1992; 26: 130–5. dence of aortic aneurysms in England and Wales. Br Med J
[223] Walker PJ, Dake MD, Mitchell RS, Miller DC. The use of 1989; 298: 33–5.
endovascular techniques for the treatment of complications [245] Meszaros I, Morocz J, Szlavi J et al. Epidemiology and
of aortic dissection. J Vasc Surg 1993; 18: 1042–51. clinicopatholology of aortic dissection. Chest 2000; 117:
[224] Williams DM, Lee DY, Hamilton BH, Marx MV, 1271–8.
Narasimham DL, Kazanjian SN, Prince MR, Andrews JC, [246] Glower DD, Speier RH, White WD, Smith LR, Rankin JS,
Cho KJ, Deeb GM The dissected aorta: percutaneous treat- Wolfe WG. Management and longterm outcome of aortic
ment of ischaemic complications — principles and results. dissection. Ann Surg 1991; 214: 31–41.
J Vasc Interv Radiol 1997; 8: 605–65. [247] Masuda Y, Takanashi K, Takasu J, Watanabe S. [Natural
[225] Dake MD, Miller DC, Semba CP, Mitchell RS, Walker PJ, history and prognosis of medical treatment for the patients
Liddell RP. Transluminal placement of endovascular stent- with aortic dissections]. Nippon Geka Gakkai Zasshi 1996;
grafts for the treatment of descending thoracic aortic 97: 890–3.
aneurysms. N Engl J Med 1994; 331: 1729–34. [248] Eagle KA, Brukmann D, Isselbacher E et al. Predictive of
[226] Slonim SM, Nyman UR, Semba CP, Miller DC, Mitchell mortality in patients with type A acute aortic dissections —
RS, Dake MD. True lumen obliteration in complicated results from the International Registry of Acute Aortic
aortic dissection: endovascular treatment. Radiology 1996; Dissection (IRAD). J Am Coll Cardiol 2000; 35: 323.
201: 161–6. [249] Wigle RL, Moran JM. Spontaneous healing of a traumatic
[227] Dake MD, Miller DC, Mitchell RS, Semba CP, Moore KA, thoracic aortic tear: case report. J Trauma 1991; 31: 280–3.
Sakai T. The ‘first generation’ of endovascular stent-grafts [250] Di Cesare E, Di Renzi P, Pavone P, Marsili L, Castallo F,
for patients with aneurysms of the descending thoracic aorta. Passariello R. Postsurgical follow-up of aortic dissections by
J Thorac Cardiovasc Surg 1998; 116: 689–703; discussion MRI. Eur J Radiol 1991; 13: 27–30.
703–4. [251] Hara K, Yamaguchi T, Wanibuchi Y, Kurokawa K. The role
[228] Nienaber CA, Fattori R, Lund G et al. Nonsurgical re- of medical treatment of distal type aortic dissection. Int J
construction of thoracic aortic dissection by stent-graft Cardiol 1991; 32: 231–40.
placement. N Engl J Med 1999; 340: 1539–45. [252] Barron DJ, Livesey SA, Brown IW, Delaney DJ, Lamb RK,
Monro JL. Twenty-year follow-up of acute type A dissec-
[229] Borst HG, Jurmann M, Buhner B, Laas J. Risk of replace-
ment of descending aorta with a standardized left heart tion: the incidence and extent of distal aortic disease using
bypass technique. J Thorac Cardiovasc Surg 1994; 107: magnetic resonance imaging. J Card Surg 1997; 12: 147–59.
126–32; discussion 132–3. [253] Masani ND, Banning AP, Jones RA, Ruttley MS, Fraser
AG. Follow-up of chronic thoracic aortic dissection: com-
[230] de Bakey ME, McCollum CH, Graham JM. Surgical treat-
parison of transesophageal echocardiography and magnetic
ment of aneurysms of the descending aorta. J Cardiovasc
resonance imaging. Am Heart J 1996; 131: 1156–63.
Surg 1978; 19: 571–6.
[254] Maffei S, Baroni M, Terrazzi M et al. Ambulatory follow-up
[231] Galloway AC, Schwartz DS, Culliford AT et al. Selective of aortic dissection: comparison between computed tomogra-
approach to descending thoracic aortic aneurysm repair: a
phy and biplane transesophageal echocardiography. Int J
ten-year experience. Ann Thorac Surg 1996; 62: 1152–7. Card Imaging 1996; 12: 105–11.
[232] Inoue K, Sato M, Iwase T et al. Clinical endovascular [255] Bogaert J, Meyns B, Rademakers FE et al. Follow-up of
placement of branched graft for type B aortic dissection. aortic dissection: contribution of MR angiography for evalu-
J Thorac Cardiovasc Surg 1996; 112: 1111–3. ation of the abdominal aorta and its branches. Eur Radiol
[233] Moon MR, Mitchell RS, Dake MD, Zarins CK, Fann JI, 1997; 7: 695–702.
Miller DC. Simultaneous abdominal aortic replacement and [256] Ide K, Uchida H, Otsuji H et al. Acute aortic dissection with
thoracic stent-graft placement for multilevel aortic disease. intramural hematoma: possibility of transition to classic
J Vasc Surg 1997; 25: 332–40. dissection or aneurysm. J Thorac Imaging 1996; 11: 46–52.
[234] Lee DY, Williams DM, Abrams GD. The dissected aorta. [257] Muluk SC, Kaufman JA, Torchiana DF, Gertler JP,
part II. Differentiation of the true from the false lumen with Cambria RP. Diagnosis and treatment of thoracic aortic
intravascular US. Radiology 1997; 203: 32–6. intramural hematoma. J Vasc Surg 1996; 24: 1022–9.
[235] Shennan T. Dissecting aneurysm. Medical Research Council [258] Murray JG, Manisali M, Flamm SD et al. Intramural
Special Report Series, No 193. London: Her Majesty’s hematoma of the thoracic aorta: MR image findings and
Stationery Office, 1984. their prognostic implications. Radiol 1997; 204: 349–55.
[236] Slonim SM, Nyman U, Semba CP, Miller DC, Mitchell RS, [259] Pepi M, Campodonico J, Galli C et al. Rapid diagnosis and
Dake MD. Aortic dissection: percutaneous management of management of thoracic aortic dissection and intamural
ischaemic complications with endovascular stents and bal- haematoma: a prospective study of advantages of multiplane
loon fenestration. J Vasc Surg 1996; 23: 241–51; discussion vs. biplane transesophageal echocardiography. Eur J
251–3. Echocardiography 2000; 1: 72–9.
[237] Murray JW, Mann JJ, Genecin A, McKusick VA. Fever with [260] Bolognesi R, Manca C, Tsialtas D et al. Aortic intramural
dissecting aneurysm of the aorta. Am J Med 1976; 61: 140–4. hematoma: an increasingly recognized aortic disease. Cardi-
[238] Link J, Muller-Hulsbeck S, Brossmann J, Steffens JC, Heller ology 1998; 89: 178–83.
M. Perivascular inflammatory reaction after percutaneous [261] Kang DH, Song JK, Song MG et al. Clinical and echo-
placement of covered stents. Cardiovasc Intervent Radiol cardiographic outcomes of aortic intramural haemorrhage
1996; 19: 345–7. compared with acute aortic dissection. Am J Cardiol 1998;
[239] Deeb GM, Williams DM, Bolling SF et al. Surgical delay for 81: 202–6.
acute type A dissection with malperfusion. Ann Thorac Surg [262] Lenferink S, Sechtem U. [Diagnosis and therapy of an
1997; 64: 1669–75; discussion 1675–7. intramural hematoma of the ascending aorta]. Dtsch Med
[240] Anagnostopoulos CE. Acute aortic dissection. Baltimore: Wschr 2000; 125: 489–92.
University Park Press, 1975. [263] Kaji S, Nishigami K, Akasaka T et al. Prediction of progres-
[241] Asfoura JY, Vidt DG. Acute aortic dissection. Chest 1991; sion or regression of type A aortic intramural haematoma by
99: 724–9. computed tomography. Circulation 1999; 100: II281–6.
[242] Fuster V, Halperin JL. Aortic dissection: a medical perspec- [264] Vilacosta I, San Roman JA, Ferreiros J, Aragoncillo P,
tive. J Card Surg 1994; 9: 713–28. Mendez R, Castillo JA, Rollan MJ, Batlle E, Peral V,

Eur Heart J, Vol. 22, issue 18, September 2001

Task Force Report 1681

Sanchez-Harguindey L. Natural history and serial mor- [280] Taylor JFN. Clinical pediatric cardiology. Curr Opin Car-
phology of aortic intramural haematoma: a novel variant of diol 1993; 8: 108–13.
aortic dissection. Am Heart J 1997; 134: 495–507. [281] Braverman AC. Exercise and the Marfan syndrome. Med Sci
[265] Coady MA, Rizzo JA, Elefteriades JA. Pathologic variants Sports Exerc 1998; 30: 387–95.
of thoracic aortic dissections. Penetrating atherosclerotic [282] Neufang KF, Theissen P, Deider S, Sechtem U. [Thoracic
ulcers and intramural haematomas. Cardiol Clin 1999; 17: aorta dissection — the place of MRT and CT in the follow-
637–57. up after prosthetic aortic replacement]. Fortschr Rontgenstr
[266] Vilacosta I, San Roman JA, Aragoncillo P et al. Penetrating 1989; 151: 659–65.
atherosclerotic aortic ulcer: documentation by transesopha- [283] Rizzo JA, Darr U, Fischer M et al. Multimodality serial
geal echocardiography. J Am Coll Cardiol 1998; 32: 83–9. follow-up of thoracic aortic aneurysms. Int J Angiol 1997; 6:
[267] Hussain S, Glover JL, Bree R, Bendick PJ. Penetrating 153–6.
atherosclerotic ulcers of the thoracic aorta. J Vasc Surg 1989;
[284] Murphy DA, Craver JM, Jones EL, Bone DK, Guyton RA,
9: 710–7.
Hatcher CR Jr. Recognition and management of ascending
[268] Ayella RJ, Hankins JR, Turney SZ, Cowley RA. Ruptured aortic dissection complicating cardiac surgical operations.
thoracic aorta due to blunt trauma. J Trauma 1977; 17: J Thorac Cardiovasc Surg 1983; 85: 247–56.
[269] Smith MD, Cassidy JM, Souther S et al. Transesophageal [285] Gott JP, Cohen CL, Jones EL. Management of ascending
aortic dissections and aneurysms early and late following
echocardiography in the diagnosis of traumatic rupture of
cardiac operations. J Card Surg 1990; 5: 2–13.
the aorta. N Engl J Med 1995; 332: 356–62.
[270] Vignon P, Gueret P, Vedrinne JM et al. Role of transesopha- [286] Suzuki S, Kondo H, Imoto K et al. [Type A acute aortic
geal echocardiography in the diagnosis and management of dissection: late reoperations for dilatation of the distal false
traumatic aortic disruption. Circulation 1995; 92: 2959–68. lumen and aortic regurgitation]. Kyobu Geka 1998; 51:
[271] Vignon P, Rambaud G, François B, Preux PM, Lang RM, 656–60.
Gastinne H. Quantification of traumatic hemomediastinum [287] Le Heuzey JY, Guize L, Guerinon J, Forman J, Sellier P,
using transesophageal echocardiography. Chest 1998; 113: Maurice P. [Dissection of the ascending aorta after aortic
1475–80. valve replacement]. Arch Mal Coeur Vaiss 1983; 76: 1349–56.
[272] Ura M, Sakata R, Nakayama Y, Goto T. Ultrasonographic [288] von Kodolitsch Y, Simic O, Schwartz A et al. Predictors of
demonstration of manipulation-related aortic injuries after proximal aortic dissection at the time of aortic valve replace-
cardiac surgery. J Am Coll Cardiol 2000; 35: 1303–10. ment. Circulation 1999; 100 II: 287–94.
[273] Groenink M, Rozendaal L, Naeff MS et al. Marfan syn- [289] Albat B, Thevenet A. Dissecting aneurysms of the ascending
drome in children and adolescents: predictive and prognostic aorta occurring late after aortic valve replacement. J Cardio-
value of aortic root growth for screening for aortic compli- vasc Surg 1992; 33: 272–5.
cations. Heart 1998; 80: 163–9. [290] Derkac W, Laks H, Cohn LH, Collins JJ Jr. Dissecting
[274] Gott VL, Greene PS, Alejo DE et al. Replacement of the aneurysms after aortic valve replacement. Arch Surg 1974;
aortic root in patients with Marfan’s syndrome. N Engl J 109: 388–90.
Med 1999; 340: 1307–13. [291] Ralph-Edwards A, David TE, Bos J. Infective endocarditis in
[275] Finkbohner R, Johnston D, Crawford ES, Coselli J, patients who had replacement of the aortic root. Ann Thorac
Milewicz DM. Marfan syndrome. Long-term survival and Surg 1994; 58: 429–32.
complications after aortic aneurysm repair. Circulation 1995; [292] Soyer R, Bessou JP, Bouchart F et al. Surgical treatment of
91: 728–33. infected composite graft after replacement of ascending
[276] Silverman DI, Burton KJ, Gray J et al. Life expectancy in the aorta. Ann Thorac Surg 1994; 58: 425–8.
Marfan syndrome. Am J Cardiol 1995; 75: 157–60. [293] Kirklin JW, Barrat-Boyes BG. In: Cardiac Surgery, 2nd edn.
[277] Crawford ES, Coselli JS. Marfan’s syndrome: combined New York: Churchill Livingstone, 1993; 2: 523–4.
composite valve graft replacement of the aortic root and
transaortic mitral valve replacement. Ann Thorac Surg 1988; [294] Karck M, Cremer J, Wawersik J, Haverich A. Reoperation
45: 296–302. for aneurysmal disease of the ascending aorta in patients
with concomitant aortic valve incompetence. J Thorac
[278] McDonald GR, Schaff HV, Pyeritz RE, McKusick VA, Gott
Cardiovasc Surg 1996; 112: 1392–3.
VL. Surgical management of patients with the Marfan syn-
drome and dilatation of the ascending aorta. J Thorac [295] Crawford ES, Crawford JL, Safi HJ, Coselli JS. Redo
Cardiovasc Surg 1981; 81: 180–6. operations for recurrent aneurysmal disease of the ascending
[279] American Academy of pediatrics Committee on Genetics. aorta and transverse aortic arch. Ann Thorac Surg 1985; 40:
Health supervision for children with Marfan syndrome. 439–55.
Pediatrics 1996; 98: 978–82.

Eur Heart J, Vol. 22, issue 18, September 2001